BIO-GENETICS LABORATORY
NPI 1164523478
Clinical Medical Laboratory in St Petersburg, FL

Q: What is Hematopathology Associates LLC's NPI number?

The NPI number for Hematopathology Associates LLC is 1164523478. It was assigned to this organization in the NPPES registry on September 26, 2006. The provider is doing business as Bio-Genetics Laboratory.

Q: What is Hematopathology Associates LLC's specialty?

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

Active since September 26, 2006

805 EXECUTIVE CENTER DR W STE 300, ST PETERSBURG, FL 33702(727) 201-1890(727) 275-1975 Get Directions Write a Review

NPPES record last updated: January 15, 2024. Verified against the NPPES registry weekly; last sync: August 02, 2026.

Record update history: Apr 14, 2021, Nov 28, 2018 (2 updates tracked since 2018).

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About Bio-genetics Laboratory NPPES

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

BIO-GENETICS LABORATORY (NPI 1164523478) is a healthcare organization registered as a clinical medical laboratory in St Petersburg, Florida and active in the NPI registry since September 2006. The organization lists Bryon Wolf, Owner, as its authorized official.

NPPES Registry Identity

NPI1164523478

Entity TypeOrganization

Primary Taxonomy291U00000X

Legal Business NameHEMATOPATHOLOGY ASSOCIATES LLC

Location Address805 EXECUTIVE CENTER DR W STE 300St Petersburg, FL 33702-2407

Mailing Address805 Executive Center Dr W Ste 300St Petersburg, FL 33702-2407 · (727) 201-1890 · Fax (727) 275-1975

Phone(727) 201-1890

Fax(727) 275-1975

Organization SubpartYes

Authorized OfficialBryon WolfOwner · (727) 201-1890

Enumeration DateSeptember 26, 2006

Last NPPES UpdateJanuary 15, 20242 updates tracked since enumeration

NPPES CertifiedJanuary 15, 2024

✔ NPI 1164523478 is a valid, active identifier and passes the ISO check-digit test.

Specialties & Licenses

★ Primary SpecialtyClinical Medical LaboratoryLaboratories

Taxonomy Code291U00000X

License✔ Licensed in FL · 800017597

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.

805 EXECUTIVE CENTER DR W STE 300, St Petersburg, FL 33702

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Other Names 1

Doing Business AsBio-genetics Laboratory

Accepted Insurance

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

Areas of Expertise CMS Part B claims 36

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.

Gene analysis (coagulation factor v) leiden variant 81241

Gene analysis for the coagulation factor V Leiden variant is a test to identify a specific genetic mutation. This mutation can increase the risk of developing abnormal blood clots in veins. The test involves analyzing a sample of your DNA, usually taken from a blood sample.

3,074 services3,074 patients

Gene analysis (prothrombin, coagulation factor ii) a variant 81240

Gene analysis for prothrombin (also known as coagulation factor II) is a test that examines your DNA to identify any variations in the prothrombin gene. These variations could potentially affect blood clotting, leading to an increased risk of certain health conditions.

2,616 services2,616 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.

2,580 services2,580 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.

2,563 services2,563 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.

2,450 services2,450 patients

Gene analysis (cytochrome p450, family 2, subfamily c, polypeptide 9) common variants 81227

Gene analysis for cytochrome P450 2C9 common variants is a test to identify specific genetic variations. These variations can affect how your body processes certain medications, helping to determine the most effective and safe drug dosage for you.

2,429 services2,429 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.

1,602 services1,602 patients

Gene analysis (runt related transcription factor 1) targeted sequence analysis 81334

Gene analysis for RUNX1 involves studying a specific part of your DNA. This test helps identify changes or mutations in the RUNX1 gene, which can provide insights into certain health conditions. It's like reading a book to find any spelling mistakes that could change the story.

1,561 services1,561 patients

Gene analysis (telomerase reverse transcriptase) targeted sequence analysis 81345

Gene analysis of telomerase reverse transcriptase (TERT) involves studying a specific segment of your DNA. It helps understand how your body's cells age and multiply, which can be crucial in diagnosing and managing certain health conditions.

1,536 services1,536 patients

Gene analysis (phosphatase and tensin homolog), full sequence analysis 81321

Gene analysis, specifically phosphatase and tensin homolog (PTEN) full sequence analysis, is a test that looks at your DNA to identify any changes in the PTEN gene. This gene helps control cell growth and division. Changes may lead to certain health conditions.

1,532 services1,532 patients

Gene analysis (bloom syndrome, recq helicase-like) 81209

Gene analysis for Bloom Syndrome involves studying the RECQ helicase-like gene. This gene is responsible for DNA repair. When it's not working properly, it can lead to Bloom Syndrome, a condition that increases the risk of developing various types of cancer.

1,515 services1,515 patients

Gene analysis (partner and localizer of brca2) full sequence analysis 81307

Gene analysis, specifically for the partner and localizer of BRCA2, involves examining your genetic code to identify any changes in this particular gene. This gene is significant in maintaining the health of your cells. The full sequence analysis means we look at every part of this gene to ensure it's working properly.

1,488 services1,488 patients

Gene analysis (coagulation factor ix) full sequence analysis 81238

Gene analysis for coagulation factor IX is a process that examines your genes, specifically the one responsible for factor IX - a protein that helps blood clot. It can detect any changes or mutations in this gene, which could affect your body's ability to control bleeding.

1,129 services1,129 patients

Gene analysis (ccaat/enhancer binding protein [c/ebp], alpha) full gene sequence 81218

Gene analysis of the CCAAT/Enhancer Binding Protein (C/EBP), Alpha, involves studying the entire sequence of this particular gene. This can help identify variations or changes in the gene that might affect your health. This process is done in a lab using a sample of your cells.

1,067 services1,067 patients

Gene analysis (v-kit hardy-zuckerman 4 feline sarcoma viral oncogene homolog), targeted sequence 81272

Gene analysis of v-kit hardy-zuckerman 4 feline sarcoma viral oncogene homolog (KIT) is a test that studies a specific gene associated with cell growth and development. It helps in identifying any alterations in this gene that may lead to health issues.

1,067 services1,067 patients

Gene analysis ((platelet-derived growth factor receptor, alpha polypeptide) targeted sequence 81314

Gene analysis for the platelet-derived growth factor receptor, alpha polypeptide (PDGFRA) involves sequencing this specific gene. The test can identify genetic changes or mutations that may cause certain health conditions. It's a non-invasive procedure that helps in early detection and personalized treatment plans.

1,067 services1,067 patients

Gene analysis (tumor protein 53) full sequence analysis 81351

Gene analysis, specifically tumor protein 53 (TP53) full sequence analysis, is a test that examines the entire TP53 gene. This gene plays a key role in preventing cancer. If there are changes or mutations in this gene, it could lead to an increased risk of developing various types of cancer.

1,067 services1,067 patients

Gene analysis (adenomatous polyposis coli), full gene sequence 81201

Gene analysis of the adenomatous polyposis coli (APC) involves studying the entire sequence of the APC gene. This test helps identify mutations that could lead to conditions like familial adenomatous polyposis. The procedure is non-invasive and uses a blood sample.

1,044 services1,044 patients

Gene analysis (nudix hydrolase 15) for common variants 81306

Gene analysis for Nudix Hydrolase 15 common variants is a genetic test that identifies changes in your NUDT15 gene. These changes can affect how your body responds to certain medications, helping your healthcare provider to personalize your treatment plan.

904 services904 patients

Gene analysis (thiopurine s-methyltransferase) for common variant 81335

Gene analysis for thiopurine S-methyltransferase (TPMT) involves studying your DNA to predict how your body might respond to certain medications. It helps in personalizing your treatment plan, reducing the risk of adverse effects.

899 services899 patients

Gene analysis (breast cancer 1 and 2) of full sequence and analysis for duplication or deletion variants 81162

Gene analysis for breast cancer 1 and 2 involves studying your DNA to detect alterations that may increase your risk of developing certain health issues. This test analyzes the full sequence and checks for duplication or deletion variants.

549 services549 patients

Gene analysis (janus kinase 2) targeted sequence analysis 81279

Gene analysis, specifically Janus Kinase 2 (JAK2) targeted sequence analysis, is a lab test that studies a specific gene in your body. It helps identify changes or mutations in the JAK2 gene, which can be linked to certain health conditions. This analysis is performed on a blood or bone marrow sample.

494 services494 patients

Gene analysis (myeloid differentiation primary response 88) for p.leu265pro variant 81305

Gene analysis for the p.Leu265Pro variant involves studying the MYD88 gene, which plays a crucial role in immune response. This test helps identify changes in this gene that could potentially cause health issues. It's a non-invasive procedure, done through a blood sample.

494 services494 patients

Gene analysis for cancer (neuroblastoma) 81311

Gene analysis for neuroblastoma is a test that studies your genes to identify abnormalities linked to this type of cancer. It helps doctors tailor treatment plans, potentially improving outcomes and reducing side effects.

494 services494 patients

Gene analysis (phospholipase c gamma 2) for common variants 81320

Gene analysis for phospholipase C gamma 2 common variants is a test that checks for changes in the PLCG2 gene. These changes can sometimes lead to certain health conditions. The test uses a sample of your body's cells to analyze your DNA.

494 services494 patients

Gene analysis (mpl proto-oncogene, thrombopoietin receptor) sequence analysis of exon 10 81339

Gene analysis of the MPL proto-oncogene, thrombopoietin receptor, specifically sequence analysis of exon 10, is a procedure that studies a specific part of your DNA. It helps to identify any changes or mutations that may contribute to certain blood disorders.

494 services494 patients

Gene analysis (glucose-6-phosphatase, catalytic subunit) common variants 81250

Gene analysis of glucose-6-phosphatase, catalytic subunit, common variants involves studying specific genes related to glucose metabolism. This helps understand if you're at risk of certain metabolic disorders. It's a non-invasive procedure, involving a simple blood or saliva sample.

479 services479 patients

Gene analysis (fanconi anemia, complementation group c) common variant 81242

Gene analysis for Fanconi Anemia, Complementation Group C, is a test that looks at your DNA to see if you have changes in a specific gene linked to this type of anemia. This can help determine if you have the condition or if you might pass it on to your children.

474 services474 patients

Gene analysis (cystic fibrosis transmembrane conductance regular) full gene sequence 81223

Gene analysis for cystic fibrosis involves examining the entire CFTR gene to identify any changes or mutations that could cause the disease. This can help in diagnosing and managing the condition effectively.

473 services473 patients

Gene analysis (glucose-6-phosphate dehydrogenase) full sequence analysis 81249

Gene analysis for glucose-6-phosphate dehydrogenase (G6PD) involves studying your DNA to check for changes in the G6PD gene. This gene controls an enzyme that helps red blood cells function properly. Anomalies can cause health issues like anemia.

473 services473 patients

Gene analysis (mutl homolog 1, colon cancer, nonpolyposis type 2) full sequence analysis 81292

Gene analysis, specifically for MUTL Homolog 1, linked to colon cancer, involves studying your DNA sequence. This helps identify any changes or mutations that might increase your risk of developing colon cancer. It's a preventive measure to manage potential health risks.

228 services228 patients

Gene analysis (muts homolog 6 [e coli]) full sequence analysis 81298

Gene analysis, specifically MUTS Homolog 6 (E. coli) full sequence analysis, is a test that examines your DNA to identify changes in the MUTS Homolog 6 gene. This information helps doctors understand and manage potential health concerns.

225 services225 patients

Gene analysis (postmeiotic segregation increased 2 [s cerevisiae]) full sequence analysis 81317

Gene analysis, specifically postmeiotic segregation increased 2 (s cerevisiae) full sequence analysis, is a scientific procedure. It involves studying your entire genetic code to identify any changes or differences that could be related to certain health conditions. This is done in a lab, using a sample provided by you.

224 services224 patients

Gene analysis (muts homolog 2, colon cancer, nonpolyposis type 1) full sequence analysis 81295

Gene analysis (MUTYH) full sequence analysis is a test that examines your DNA to identify any changes linked to nonpolyposis colon cancer type 1. This can help determine your risk of developing this type of cancer.

221 services221 patients

Gene analysis (cytochrome p450 family 3 subfamily a member 5) for common variant 81231

Gene analysis for the cytochrome P450 3A5 variant helps understand your body's response to certain medications. It's a genetic test that examines how your body metabolizes drugs, aiding in personalized medication plans.

32 services32 patients

Gene analysis (dihydropyrimidine dehydrogenase) for common variant 81232

Gene analysis for dihydropyrimidine dehydrogenase (DPD) common variant involves studying a specific gene in your body. This gene affects how your body processes certain medications. The test identifies any changes in this gene which may influence your response to these medications.

32 services32 patients

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 Hematopathology Associates LLC's NPI number?

The NPI number for Hematopathology Associates LLC is 1164523478. It was assigned to this organization in the NPPES registry on September 26, 2006. The provider is doing business as Bio-Genetics Laboratory.

Where is Hematopathology Associates LLC located?

Hematopathology Associates LLC is located at 805 Executive Center Dr W Ste 300, St Petersburg, FL 33702. The listed phone number is (727) 201-1890.

What is Hematopathology Associates LLC's specialty?

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

What insurance does Hematopathology Associates LLC accept?

Health plans from Ambetter Health, Ambetter from Buckeye Health Plan, Ambetter from Meridian and Blue Cross Blue Shield of Arizona list Hematopathology Associates 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 Hematopathology Associates LLC was last updated on January 15, 2024. NPI Profile syncs weekly with the NPPES registry data releases published by CMS. This NPI record was last updated 2 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.