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Results: 1 to 20 of 40

Tests names and labsConditionsGenes, analytes, and microbesMethods

Common Hereditary Cancer Screening Panel

PreventionGenetics
United States
9455
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Invitae Multi-Cancer + RNA Panel

Invitae
United States
14363
  • D Deletion/duplication analysis

Invitae Common Hereditary Cancers + RNA Panel

Invitae
United States
11447
  • D Deletion/duplication analysis

Mismatch Repair Proteins by Immunohistochemistry

GoPath Laboratories, LLC
United States
64
  • I Immunohistochemistry

Oligodontia-colorectal cancer syndrome, 608615, Autosomal dominant; ODCRCS (Oligodontia-cancer predisposition syndrome) (AXIN2 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetic Diagnosis and Research Centre
Turkey
11
  • C Sequence analysis of the entire coding region

Aventus GenSeq

Aventus Biolabs
United States
66133
  • C Sequence analysis of the entire coding region

Pediatric Cancer Panel

PreventionGenetics
United States
7864
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Oligodontia - Selective tooth agenesis Deletion / Duplication panel

HNL Genomics Connective Tissue Gene Tests
United States
109
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Oligodontia - Selective tooth agenesis NGS panel

HNL Genomics Connective Tissue Gene Tests
United States
109
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Oligodontia - Selective tooth agenesis Comprehensive panel

HNL Genomics Connective Tissue Gene Tests
United States
109
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Tooth Agenesis Panel

PreventionGenetics
United States
159
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Invitae Ectodermal Dysplasia and Related Disorders Panel

Invitae
United States
14873
  • D Deletion/duplication analysis

Colorectal Cancer Panel

PreventionGenetics
United States
3225
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Cancer Panel

PreventionGenetics
United States
122117
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Oligodontia-Colorectal Cancer via the AXIN2 Gene

PreventionGenetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Inherited Cancer Panel

Dhiti Omics Technologies Private Ltd
India
13684
  • C Sequence analysis of the entire coding region

Hereditary pediatric cancer panel. NGS panel of 71 genes.

Genologica Medica
Spain
15871
  • C Sequence analysis of the entire coding region

VistaSeq Comprehensive Cancer Panel

Molecular Diagnostic Laboratory LabCorp
United States
4758
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary colon cancer (NGS panel for 21 genes, including CNV analysis)

Unilabs Genetics CGC Genetics
Portugal
4921
  • C Sequence analysis of the entire coding region

Colorectal cancer (WES based NGS panel of 30 genes, including CNV analysis)

Unilabs Genetics CGC Genetics
Portugal
5630
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 40

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.