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Results: 1 to 20 of 90

Tests names and labsConditionsGenes, analytes, and microbesMethods

CancerNext® 37

Ambry Genetics
United States
7937
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Variant Resolution Test for CancerNext® 37 (+RNAinsight®)

Ambry Genetics
United States
7918
  • D Deletion/duplication analysis
  • R RNA analysis
  • C Sequence analysis of the entire coding region

Endeavor

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

Variant Resolution Test for Penn Cancer Grant Panel (+RNAinsight®)

Ambry Genetics
United States
7918
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Penn Cancer Grant Panel

Ambry Genetics
United States
7980
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

BRCANext-Expanded™

Ambry Genetics
United States
3520
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

BRCANext™

Ambry Genetics
United States
3518
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Squamous cell carcinoma, head and neck, somatic, 275355 (Squamous cell carcinoma of head and neck) (ING1 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Squamous cell carcinoma, head and neck, 275355, Autosomal recessive; HNSCC (Squamous cell carcinoma of head and neck) (TNFRSF10B gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Squamous cell carcinoma, head and neck, somatic, 275355 (Squamous cell carcinoma of head and neck) (PTEN gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

KRAS, BRAF, and NRA Mutation Analysis

PathGroup
United States
233
  • T Targeted variant analysis

KRAS, BRAF, NRAS and MSI Mutation Analysis

PathGroup
United States
233
  • T Targeted variant analysis

BRAF, EGFR, KRAS Mutation Analysis

PathGroup
United States
253
  • T Targeted variant analysis

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 MelanomaNext® (+RNAinsight®)

Ambry Genetics
United States
403
  • D Deletion/duplication analysis
  • R RNA analysis
  • C Sequence analysis of the entire coding region

Variant Resolution Test for BrainTumorNext® (+RNAinsight®)

Ambry Genetics
United States
728
  • D Deletion/duplication analysis
  • R RNA analysis
  • C Sequence analysis of the entire coding region

Variant Resolution Test for ColoNext® (+RNAinsight®)

Ambry Genetics
United States
4810
  • D Deletion/duplication analysis
  • R RNA analysis
  • C Sequence analysis of the entire coding region

Variant Resolution Test for RenalNext® (+RNAinsight®)

Ambry Genetics
United States
577
  • 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

PrimBio Cancer HotSpot Panel

PrimBio Research Institute
United States
6050
  • T Targeted variant analysis

Results: 1 to 20 of 90

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.