INNOVATIVE GENOMICS LLC
NPI 1629531769
Clinical Medical Laboratory in San Antonio, TX

Q: What is Innovative Genomics LLC's NPI number?

The NPI number for Innovative Genomics LLC is 1629531769. It was assigned to this organization in the NPPES registry on April 6, 2019.

Q: What is Innovative Genomics LLC's specialty?

The primary specialty registered for this NPI is Clinical Medical Laboratory with taxonomy code 291U00000X.

Active since April 06, 2019

5410 FREDERICKSBURG RD, SUITE 304, SAN ANTONIO, TX 78229(210) 352-5175 Get Directions Write a Review

NPPES record last updated: May 20, 2020. Verified against the NPPES registry weekly; last sync: August 02, 2026.

Record update history: May 20, 2020, Mar 16, 2020, Jun 7, 2019 and 1 more (4 updates tracked since 2019).

On this page

About Innovative Genomics Llc NPPES

Official registry information on file with the National Plan and Provider Enumeration System.

INNOVATIVE GENOMICS LLC (NPI 1629531769) is a healthcare organization registered as a clinical medical laboratory in San Antonio, Texas and active in the NPI registry since April 2019. The organization lists Diego Sanchez Sanudo Chocron, Cfo, as its authorized official.

NPPES Registry Identity

NPI1629531769

Entity TypeOrganization

Primary Taxonomy291U00000X

Legal Business NameINNOVATIVE GENOMICS LLC

Location Address5410 FREDERICKSBURG RD, SUITE 304San Antonio, TX 78229

Mailing Address5410 Fredericksburg Rd Ste 304San Antonio, TX 78229-3576 · (210) 351-5175 · Fax (210) 352-5175

Phone(210) 352-5175

Organization SubpartNo

Authorized OfficialDiego Sanchez Sanudo ChocronCfo · (310) 985-2834

Enumeration DateApril 6, 2019

Last NPPES UpdateMay 20, 20204 updates tracked since enumeration

NPPES CertifiedMay 20, 2020

✔ NPI 1629531769 is a valid, active identifier and passes the ISO check-digit test.

Specialties & Licenses

★ Primary SpecialtyClinical Medical LaboratoryLaboratories

Taxonomy Code291U00000X

Definition

(1) A clinical laboratory is a facility for the biological, microbiological, serological, chemical, immunohematological, hematological, biophysical, cytological, pathological, or other examination of materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of any disease or impairment of, human beings. These examinations also include procedures to determine, measure, or otherwise describe the presence or absence of various substances or organisms in the body. Facilities only collecting or preparing specimens (or both) or only serving as a mailing service and not performing testing are not considered clinical laboratories. (2) Any facility that examines materials from the human body for purposes of providing information for the diagnosis, prevention, or treatment of any disease or impairment of, or the assessment of, the health of human beings. Typical divisions of a clinical laboratory include hematology, cytology, bacteriology, histology, biochemistry, medical toxicology, and serology.

5410 FREDERICKSBURG RD, San Antonio, TX 78229

Open in Google Maps ↗

Other Identifiers 1

Other45D2155835TX · Clia

Accepted Insurance

The full list of accepted plans is on the Insurance tab. Issuers include Ambetter from Absolute Total Care, Ambetter from Buckeye Health Plan, Ambetter from Meridian and more.Insurance ›

Areas of Expertise CMS Part B claims 52

Services this provider delivered to Medicare fee-for-service patients, from the CMS Medicare utilization data. Higher counts generally reflect more experience with a service; care delivered outside Medicare is not included.

Detection test by nucleic acid for organism, amplified probe technique 87798

A nucleic acid detection test is a procedure to identify specific organisms in your body. This test uses an amplified probe technique, which magnifies the genetic material of the organism, making it easier to detect. It's a precise way to diagnose infections.

5,355 services405 patients

Detection test for candida species (yeast), amplified probe technique 87481

This test helps identify Candida, a type of fungus often present in the human body. An amplified probe technique is used, which enhances detection of the fungus in a sample. This method increases the accuracy of the test, helping to determine the best treatment.

1,720 services331 patients

Detection test by nucleic acid for vancomycin resistance strep (vre), amplified probe technique 87500

The detection test by nucleic acid for vancomycin-resistant strep (VRE) is a laboratory procedure. It uses an amplified probe technique to identify specific genetic material in bacteria. This helps determine if the bacteria are resistant to the antibiotic vancomycin.

411 services374 patients

Detection test by nucleic acid for staphylococcus aureus (bacteria), amplified probe technique 87640

A detection test for Staphylococcus aureus uses a method called the amplified probe technique. This method identifies the bacteria's unique genetic material, or nucleic acid, helping to confirm its presence. It's a highly accurate way to detect this type of bacteria.

411 services374 patients

Detection test by nucleic acid for strep (streptococcus, group a), amplified probe technique 87651

This test detects Group A Streptococcus bacteria in your body. It uses an amplified probe technique, which amplifies the bacteria's nucleic acid, making it easier to identify. This test helps diagnose conditions like strep throat or scarlet fever.

411 services374 patients

Detection test by nucleic acid for staphylococcus aureus, methicillin resistant (mrsa bacteria), amplified probe technique 87641

A detection test by nucleic acid for MRSA bacteria uses an amplified probe technique. It's a lab procedure that identifies the presence of MRSA, a type of bacteria resistant to many antibiotics. This test helps in deciding the best treatment.

347 services311 patients

Detection test by nucleic acid for strep (streptococcus, group b), amplified probe technique 87653

A detection test by nucleic acid for Group B Strep uses an amplified probe technique. This test identifies the presence of Group B Strep bacteria in the body. It involves collecting a sample, usually a swab, which is then examined in a lab for the bacteria's genetic material.

224 services196 patients

Detection test by nucleic acid for mycobacteria species (bacteria), amplified probe technique 87551

This test identifies the presence of mycobacteria species, which can cause various infections including tuberculosis. It uses a technique called amplified probe, which magnifies the bacteria's nucleic acid, making it easier to detect.

180 services127 patients

Detection test by nucleic acid for herpes simplex virus, amplified probe technique 87529

This test uses an amplified probe technique to identify the presence of the herpes simplex virus in your body. It works by detecting the virus's genetic material, or nucleic acid. The test is accurate, reliable, and can help in early detection and treatment.

126 services63 patients

Manual urinalysis test with examination using microscope, automated 81001

A manual urinalysis test with automated microscopic examination is a lab process that checks your urine for health indicators. It involves a machine scanning your sample to identify any abnormal elements, which can assist in diagnosing various conditions.

79 services67 patients

Detection test by nucleic acid for legionella pneumophila (water borne bacteria), amplified probe technique 87541

A detection test for Legionella Pneumophila, a waterborne bacteria, uses the amplified probe technique. This involves identifying the bacteria's unique genetic material (nucleic acid) and amplifying it for easier detection, aiding in accurate diagnosis.

77 services75 patients

Detection test by nucleic acid for mycoplasma pneumoniae (bacteria), amplified probe technique 87581

This test checks for Mycoplasma pneumoniae, a bacteria that can cause lung infection. It uses a method called amplified probe technique, which identifies the bacteria's genetic material. This helps in diagnosing the infection accurately.

77 services75 patients

Gene analysis (5, 10-methylenetetrahydrofolate reductase) common variants 81291

Gene analysis for 5,10-methylenetetrahydrofolate reductase (MTHFR) common variants is a test that looks at your DNA to identify any changes in the MTHFR gene. These changes can affect how your body processes certain vitamins, which could impact your overall health.

59 services59 patients

Detection test by nucleic acid for multiple types of respiratory virus, multiple types or subtypes, 3-5 targets 87631

This test identifies different respiratory viruses by examining their nucleic acid, the building blocks of their genetic material. It can detect multiple types or subtypes, specifically 3-5 targets. This helps in diagnosing your respiratory illness accurately.

52 services51 patients

Detection by nucleic acid bartonella henselae and bartonella quintana (bacteria), amplified probe technique 87471

This is a lab test that identifies Bartonella Henselae and Bartonella Quintana bacteria in your body. The amplified probe technique is used to increase the amount of bacterial DNA, making it easier to detect. This helps in diagnosing diseases caused by these bacteria.

50 services50 patients

Detection test by nucleic acid for mycobacteria avium-intracellulare (bacteria), amplified probe technique 87561

This test identifies the presence of Mycobacteria Avium-Intracellulare, bacteria often linked with lung diseases. The amplified probe technique enhances the detection process by amplifying the bacteria's nucleic acid, making it easier to spot.

47 services47 patients

Gene analysis (fragile x intellectual disability 2) for detection of abnormal alleles 81171

Gene analysis for Fragile X Mental Retardation 2 involves studying your genetic material to identify any unusual changes in a specific gene. This can help determine if you have a particular genetic condition, or if you might pass it on to your children.

38 services38 patients

Gene analysis (atropin 1) for abnormal alleles 81177

Gene analysis for Atropin 1 involves studying your DNA to identify any unusual genetic variations. This test helps in understanding your genetic makeup better, which can aid in diagnosing or predicting certain health conditions.

38 services38 patients

Gene analysis (ataxin 1) for abnormal alleles 81178

Gene analysis of ataxin 1 involves studying your DNA to identify any abnormal versions of the ataxin 1 gene. This gene is associated with certain neurological disorders. The test helps in early detection and management of these conditions.

38 services38 patients

Gene analysis (ataxin 2) for abnormal alleles 81179

Gene analysis for ataxin 2 checks for alterations in the ATXN2 gene. This gene is responsible for producing a protein essential for normal cell functions. If abnormal, it may lead to certain neurological disorders. The test involves analyzing your DNA, typically obtained via a blood sample.

38 services38 patients

Gene analysis (ataxin 3) for abnormal alleles 81180

Gene analysis for ataxin 3 helps identify abnormal alleles, or variations, in the ataxin 3 gene. This gene plays a role in neurological function. If abnormal, it may indicate conditions like Machado-Joseph disease. The process involves analyzing a blood sample.

38 services38 patients

Gene analysis (ataxin 7) for abnormal alleles 81181

Gene analysis for ataxin 7 involves studying your DNA to identify any unusual changes in the ataxin 7 gene. These changes, known as abnormal alleles, can cause health conditions like spinocerebellar ataxia. The test helps in early detection and management.

38 services38 patients

Gene analysis (ataxin 8 opposite strand [non-protein coding]) for abnormal alleles 81182

Gene analysis for ataxin 8 opposite strand checks for unusual gene variants. This test helps identify genetic conditions that could affect your health. It involves analyzing your DNA, usually from a blood sample, to find these abnormal alleles.

38 services38 patients

Gene analysis (ataxin 10) for abnormal alleles 81183

Gene analysis for ataxin 10 involves examining your DNA to identify any abnormal versions of the ataxin 10 gene. These abnormalities could potentially cause certain health conditions. This test is non-invasive and helps in early detection and management of these conditions.

38 services38 patients

Gene analysis (calcium voltage-gated channel subunit alpha1 a) of full sequence 81185

Gene analysis of the calcium voltage-gated channel subunit alpha1 a involves examining your DNA to understand how your body regulates calcium. This helps identify potential health risks related to calcium imbalances. It's a non-invasive procedure involving a simple blood or saliva sample.

38 services38 patients

Gene analysis (cystatin b) of full sequence 81189

Gene analysis of the full sequence of Cystatin B is a test that examines your DNA to identify any changes in the Cystatin B gene. This gene is linked to certain health conditions. The analysis helps in diagnosing and tailoring treatment plans.

38 services38 patients

Gene analysis (neurotrophic receptor tyrosine kinase 1) translocation analysis 81191

Gene analysis, specifically neurotrophic receptor tyrosine kinase 1 (NTRK1) translocation analysis, is a test that examines your genes for specific changes. These changes could potentially lead to certain health conditions. This analysis helps in providing personalized treatment plans.

38 services38 patients

Gene analysis (neurotrophic receptor tyrosine kinase 2) translocation analysis 81192

Gene analysis, specifically neurotrophic receptor tyrosine kinase 2 (NTRK2) translocation analysis, is a test that studies alterations in your genes. This analysis helps identify changes in the NTRK2 gene, which can sometimes be linked to certain health conditions. It's a vital part of personalized medicine.

38 services38 patients

Gene analysis (aspartoacylase) 81200

Gene analysis for aspartoacylase is a test that studies your DNA to check for mutations in the ASPA gene. This gene is responsible for producing an enzyme called aspartoacylase, which plays a crucial role in brain development and function. Any changes could lead to health issues.

38 services38 patients

Gene analysis (fragile x syndrome, x-linked intellectual disability) for detection of abnormal alleles 81243

Gene analysis for Fragile X Mental Retardation involves studying your DNA to identify any abnormal changes or 'alleles'. This helps in detecting the presence of Fragile X syndrome, a genetic condition that can cause learning and behavioral challenges.

38 services38 patients

Gene analysis (huntingtin) for abnormal alleles 81271

Gene analysis for huntingtin examines your DNA to identify if you have abnormal versions of the huntingtin gene. These abnormal genes are associated with Huntington's disease, a nervous system disorder. This test helps in early detection and management.

38 services38 patients

Gene analysis (partner and localizer of brca2) targeted sequence analysis 81309

Gene analysis, specifically the partner and localizer of BRCA2 targeted sequence analysis, is a scientific procedure that studies specific parts of your DNA. It helps to identify if you have certain genetic changes that may increase your risk of developing specific health conditions.

38 services38 patients

Gene analysis (poly[a] binding protein nuclear 1) for abnormal alleles 81312

Gene analysis for Poly(A) Binding Protein Nuclear 1 (PABPN1) checks for abnormal alleles or variations in your DNA. This test can help identify genetic disorders caused by these variations. It's a non-invasive procedure, involving a simple blood or saliva sample.

38 services38 patients

Gene analysis (peripheral myelin protein 22), full sequence analysis 81325

Gene analysis of peripheral myelin protein 22 involves studying the full sequence of this specific gene. This analysis helps identify any genetic variations that may lead to certain health conditions. It's a non-invasive test involving a simple blood draw or saliva sample.

38 services38 patients

Gene analysis (survival of motor neuron 1, telomeric) of full sequence 81336

Gene analysis of the full sequence of Survival of Motor Neuron 1 (telomeric) is a test that examines your DNA to identify any changes in this specific gene. These changes could indicate conditions like Spinal Muscular Atrophy. It's a non-invasive procedure.

38 services38 patients

Gene analysis (protein phosphatase 2 regulatory subunit bbeta) for abnormal alleles 81343

Gene analysis for the protein phosphatase 2 regulatory subunit Bbeta checks for unusual variations in your genes. This helps to identify potential health issues related to these genes. It's a simple, non-invasive test using a blood or saliva sample.

38 services38 patients

Gene analysis (tata box binding protein) for abnormal alleles 81344

Gene analysis for the TATA box binding protein checks for abnormal alleles or variations in your DNA. This analysis helps identify potential genetic conditions. It's done by examining a sample of your cells, typically obtained through a blood draw or a cheek swab.

38 services38 patients

Gene analysis (methyl cpg binding protein 2) full sequence analysis 81302

Gene analysis, specifically Methyl CpG Binding Protein 2 (MECP2) full sequence analysis, is a detailed examination of your DNA. This test focuses on the MECP2 gene, which plays a crucial role in nerve cell function and development. The results can help identify alterations or mutations that may cause certain health conditions.

37 services37 patients

Hla class i typing high resolution one locus 81380

HLA Class I Typing High Resolution One Locus is a detailed genetic test. It identifies specific proteins on your cells to help match organ or bone marrow donors and recipients. This ensures the body accepts the transplant.

37 services37 patients

Molecular pathology procedure level 1 81400

A Molecular Pathology Procedure Level 1 is a lab test that studies the genes in your cells. It helps identify alterations in your DNA that may cause or contribute to certain diseases. The procedure is non-invasive and helps in early disease detection.

37 services37 patients

Gene analysis (hemochromatosis) common variants 81256

Gene analysis for hemochromatosis common variants is a test that checks for specific changes in your DNA. These changes could indicate a higher risk of developing hemochromatosis, a condition that causes your body to absorb too much iron from your diet.

34 services34 patients

Gene analysis (frataxin) of full sequence 81286

Gene analysis of frataxin involves studying the entire sequence of the frataxin gene. This test helps identify any changes or mutations in the gene that may cause health issues, such as Friedreich's ataxia. It's a non-invasive procedure using a blood sample.

33 services33 patients

Detection test by nucleic acid for mycobacteria tuberculosis (tb bacteria), amplified probe technique 87556

A detection test by nucleic acid for Mycobacteria Tuberculosis, using an amplified probe technique, is a diagnostic test for TB. It identifies the TB bacteria's genetic material in your body. It's fast, highly accurate, and can confirm TB presence even in small samples.

31 services31 patients

Amplifed dna or rna probe detection of severe acute respiratory syndrome coronavirus 2 (covid-19) antigen 87635

This is a lab test that detects the presence of COVID-19 in your body. It uses a technique to amplify the virus's genetic material, either DNA or RNA, making it easier to identify. A positive result indicates an active infection.

24 services23 patients

Gene analysis (solute carrier organic anion transporter family, member 1b1) for common variant 81328

Gene analysis for the solute carrier organic anion transporter family, member 1b1 (SLCO1B1), common variant, is a test that examines your DNA to identify variations in the SLCO1B1 gene. This gene plays a crucial role in the body's ability to process certain medications.

19 services19 patients

Gene analysis (cytochrome p450, family 2, subfamily c, polypeptide 19) common variants 81225

Gene analysis of cytochrome P450 2C19 common variants is a test that helps understand how your body processes certain medications. This can help your doctor tailor treatments specifically for you, improving their effectiveness and safety.

16 services16 patients

Detection test by nucleic acid for chlamydia pneumoniae, amplified probe technique 87486

This test checks for the presence of Chlamydia pneumoniae, a bacterium that can cause respiratory infections. It uses an amplified probe technique, which magnifies the bacterium's genetic material for easier detection. It's a standard, non-invasive procedure.

13 services13 patients

Detection of mycoplasma genitalium by dna or rna probe 87563

This procedure involves the use of special probes to identify the presence of a specific bacteria, Mycoplasma Genitalium, in your body. These probes detect the bacteria's unique DNA or RNA, helping to confirm if you have an infection.

12 services12 patients

Detection test by nucleic acid for trichomonas vaginalis (genital parasite), amplified probe technique 87661

This is a test to identify a common microscopic organism that can cause discomfort. The technique involves using a special probe to amplify the organism's genetic material, making it easier to detect. It's a simple, safe, and accurate procedure.

12 services12 patients

Gene analysis (cytochrome p450, family 2, subfamily d, polypeptide 6) common variants 81226

Gene analysis of cytochrome P450 2D6 (CYP2D6) common variants involves studying specific genes to understand your body's ability to process certain medications. This can help tailor treatments to your unique genetic makeup, optimizing medication effectiveness and safety.

11 services11 patients

Detection test by nucleic acid for chlamydia trachomatis, amplified probe technique 87491

A detection test by nucleic acid for chlamydia trachomatis, amplified probe technique, is a test that identifies the presence of a specific bacteria in the body. This bacteria can cause various health issues. The technique amplifies the sample to improve accuracy.

11 services11 patients

Detection test by nucleic acid for neisseria gonorrhoeae (gonorrhoeae bacteria), amplified probe technique 87591

This is a lab test that checks for the presence of a specific bacteria called Neisseria gonorrhoeae in your body. It uses a technique called amplified probe, which makes many copies of the bacteria's genetic material (nucleic acid) to help detect it more easily.

11 services11 patients

Leave this field empty

Other Providers at the Same Location NPPES 13

Providers registered at the same practice address, or within the immediate area, according to the NPPES registry.

SAN ANTONIO INJURY REHABILITATION

Occupational Therapist

5410 FREDERICKSBURG RD, SUITE 102
SAN ANTONIO, TX 78229

Bexar County (210) 692-7860

SABRINA ESPARZA PTA

Physical Therapy Assistant

5410 FREDERICKSBURG RD
SAN ANTONIO, TX 78229

Bexar County (210) 551-0085

AMEDISYS TEXAS LLC

Home Health

5410 FREDERICKSBURG RD, SUITE 306
SAN ANTONIO, TX 78229

Bexar County (210) 340-0294

SAN ANTONIO INTERDISCIPLINARY PAIN ALLIANCE

Occupational Therapist

5410 FREDERICKSBURG RD, SUITE 102
SAN ANTONIO, TX 78229

Bexar County (210) 692-7860

MR. GREG MCNEELY O.T.R.

Occupational Therapist

5410 FREDERICKSBURG RD, SUITE 102
SAN ANTONIO, TX 78229

Bexar County (210) 702-3401

OSCAR J CERDA MD

Family Medicine

5410 FREDERICKSBURG RD, SUITE 112
SAN ANTONIO, TX 78229

Bexar County (210) 733-3008

MR. JOHN WOODROW CLARK PTA

Physical Therapy Assistant

5410 FREDERICKSBURG RD, SUITE 306 INTELISTAF HEALTHCARE
SAN ANTONIO, TX 78229

Bexar County (210) 384-0115

KAREN DIANE KEELER P.T.

Physical Therapist

5410 FREDERICKSBURG RD, SUITE 100
SAN ANTONIO, TX 78229

Bexar County (210) 541-0058

Frequently Asked Questions NPPES & CMS

Common questions about this NPI record, answered from the official NPPES registry and CMS datasets shown on this page.

What is Innovative Genomics LLC's NPI number?

The NPI number for Innovative Genomics LLC is 1629531769. It was assigned to this organization in the NPPES registry on April 6, 2019.

Where is Innovative Genomics LLC located?

Innovative Genomics LLC is located at 5410 Fredericksburg Rd Suite 304, San Antonio, TX 78229. The listed phone number is (210) 352-5175.

What is Innovative Genomics LLC's specialty?

The primary specialty registered for this NPI is Clinical Medical Laboratory with taxonomy code 291U00000X.

What insurance does Innovative Genomics LLC accept?

Health plans from Ambetter Health, Ambetter from Absolute Total Care, Ambetter from Buckeye Health Plan, Ambetter from Meridian and Ambetter of Alabama and 6 other insurers list Innovative Genomics LLC as in-network in at least one marketplace plan. Coverage varies by plan and year; verify with the insurer or the provider before a visit.

When was this NPI record last updated?

The NPPES record for Innovative Genomics LLC was last updated on May 20, 2020. NPI Profile syncs weekly with the NPPES registry data releases published by CMS. This NPI record was last updated 6 years ago. If this record has changed at CMS more recently, you can request an on-demand re-check against the live CMS registry, directly from this page.