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Results: 1 to 20 of 231

Tests names and labsConditionsGenes, analytes, and microbesMethods

Expedio Hereditary Cancer Predisposition Screening Assay

Kailos Genetics
United States
4031
  • C Sequence analysis of the entire coding region

Shield™ test

Guardant Health
United States
11
  • M Methylation analysis
  • E Sequence analysis of select exons

OnkoRisk Hereditary Oncology Plus Panel

BioReference Health
United States
9777
  • C Sequence analysis of the entire coding region

OnkoRisk Hereditary Oncology Management Panel

BioReference Health
United States
4717
  • C Sequence analysis of the entire coding region

OnkoRisk Hereditary Oncology Guideline Panel

BioReference Health
United States
7154
  • C Sequence analysis of the entire coding region

OnkoRisk Women's Hereditary Cancer Panel

BioReference Health
United States
3418
  • C Sequence analysis of the entire coding region

OnkoRisk Hereditary Urology Panel

BioReference Health
United States
2719
  • C Sequence analysis of the entire coding region

Guardant Shield LDT

Guardant Health
United States
11
  • P Protein analysis
  • M Methylation analysis
  • E Sequence analysis of select exons

Tumor, Microsatellite Instability

Mayo Clinic Laboratories Mayo Clinic
United States
11
  • I Microsatellite instability testing (MSI)

KRAS Mutation Analysis

PathGroup
United States
131
  • T Targeted variant analysis

Otogenetics Hereditary Cancers

Otogenetics
United States
3639
  • E Sequence analysis of select exons

Birt-Hogg-Dube syndrome

Molecular Genetics Laboratory North York General Hospital
Canada
31
  • C Sequence analysis of the entire coding region

Polyposis panel (18 genes)

Molecular Genetics Laboratory North York General Hospital
Canada
1018
  • C Sequence analysis of the entire coding region

Hereditary breast, ovarian, prostate, GI cancer panel (36 genes)

Molecular Genetics Laboratory North York General Hospital
Canada
1836
  • C Sequence analysis of the entire coding region

Hereditary GI cancer panel (31 genes)

Molecular Genetics Laboratory North York General Hospital
Canada
1331
  • C Sequence analysis of the entire coding region

Invitae Expanded Renal Disease Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
693388
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae eMERGE Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
5916
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Adenomatous Polyposis Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
72
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Tier 1 Hereditary Conditions Test

Color Diagnostics, LLC DBA Color Health
United States
1410
  • C Sequence analysis of the entire coding region

cfDNA KRAS 12, 13, 61, 146 Blood

Mayo Clinic Laboratories Mayo Clinic
United States
11
  • T Targeted variant analysis

Results: 1 to 20 of 231

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.