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Results: 1 to 20 of 63

Tests names and labsConditionsGenes, analytes, and microbesMethods

PREVENTEST

GeneID Lab - Advanced Molecular Diagnostics
United States
6034
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

OncoAlly™ BRCA1/2 Analysis Analysis

Variantyx, Inc.
United States
22
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Custom Gene Panel, Hereditary

Mayo Clinic Laboratories Mayo Clinic
United States
22
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Custom Panel (Cancer Genetics)

PreventionGenetics, part of Exact Sciences
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Variant Resolution Test for CancerNext® (+RNAinsight®)

Ambry Genetics
United States
5534
  • D Deletion/duplication analysis
  • R RNA analysis
  • C Sequence analysis of the entire coding region

Variant Resolution Test for CustomNext-Cancer® (+RNAinsight®)

Ambry Genetics
United States
14718
  • D Deletion/duplication analysis
  • R RNA analysis
  • C Sequence analysis of the entire coding region

Variant Resolution Test for CancerNext-Expanded® (+RNAinsight®)

Ambry Genetics
United States
9571
  • D Deletion/duplication analysis
  • R RNA analysis
  • C Sequence analysis of the entire coding region

CustomNext-Cancer®

Ambry Genetics
United States
14791
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CancerNext-Expanded®

Ambry Genetics
United States
12271
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Bone Marrow Failure Panel, Sequencing and Deletion/Duplication

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
5075
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

OncoAlly™ Cancer Predisposition

Variantyx, Inc.
United States
287
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Hereditary Cancer Panel

NxGen MDx
United States
3232
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

OncoGeneDx Custom Panel

GeneDx
United States
10382
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Common Cancer Management Panel

GeneDx
United States
5637
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Breast/Gyn Cancer Panel

GeneDx
United States
4624
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Common Cancer Panel

GeneDx
United States
6047
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

ACMG Secondary Findings (Medically Actionable Genes, Including Cardio and Cancer) NGS Panel

Fulgent Genetics
United States
17759
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Breast and Ovarian Cancer Comprehensive Panel

Fulgent Genetics
United States
5824
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Full Focus Cancer Panel

Fulgent Genetics
United States
8230
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Cancer High Risk Panel

Blueprint Genetics
Finland
128
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 63

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.