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Results: 1 to 20 of 35

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

Hereditary Cancer Panel Comprehensive

Molecular Genetics Laboratory London Health Sciences Centre
Canada
3930
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

BRCA2-Hereditary Cancer of the Breast

Molecular Genetics Laboratory London Health Sciences Centre
Canada
51
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

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

Otogenetics Hereditary Cancers

Otogenetics
United States
3639
  • E Sequence analysis of select exons

BRCA2 Gene Sequencing

Michigan Medical Genetics Laboratories University of Michigan
United States
71
  • C Sequence analysis of the entire coding region

BRCA2 deletion/duplication testing

Michigan Medical Genetics Laboratories University of Michigan
United States
61
  • D Deletion/duplication analysis

BRCA1 gene sequencing

Michigan Medical Genetics Laboratories University of Michigan
United States
71
  • C Sequence analysis of the entire coding region

BRCA1 deletion/duplication testing

Michigan Medical Genetics Laboratories University of Michigan
United States
71
  • D Deletion/duplication analysis

BRCA1 and BRCA2 Sequencing and Del/Dup

Michigan Medical Genetics Laboratories University of Michigan
United States
82
  • C Sequence analysis of the entire coding region

Li Fraumeni Syndrome

Molecular Genetics Laboratory London Health Sciences Centre
Canada
51
  • 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

Endeavor

PathGroup
United States
73505
  • C Sequence analysis of the entire coding region

Hereditary Cancer Test

Color Diagnostics, LLC DBA Color Health
United States
2429
  • C Sequence analysis of the entire coding region

Hereditary breast/ovarian cancer - analysis the BRCA1 gene mutations in accordance with EMQN recommendations

Laboratory of Human Genetics GENOMED Health Care Center
Poland
61
  • C Sequence analysis of the entire coding region

Hereditary breast/ovarian cancer - analysis the BRCA2 gene mutations in accordance with EMQN recommendations

Laboratory of Human Genetics GENOMED Health Care Center
Poland
61
  • C Sequence analysis of the entire coding region

Hereditary Disease Risk Test

Color Diagnostics, LLC DBA Color Health
United States
5159
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 35

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.