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Results: 1 to 20 of 78

Tests names and labsConditionsGenes, analytes, and microbesMethods

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

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

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 CancerNext-Expanded® (+RNAinsight®)

Ambry Genetics
United States
8890
  • 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

PTEN gene sequence and deletion/duplication

Ambry Genetics
United States
111
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CustomNext-Cancer®

Ambry Genetics
United States
9490
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CancerNext-Expanded®

Ambry Genetics
United States
8689
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PTEN Sequence Analysis (Prenatal Diagnosis)

Baylor Genetics
United States
81
  • T Targeted variant analysis

PTEN Sequence Analysis (Familial Mutation/Variant Analysis)

Baylor Genetics
United States
81
  • T Targeted variant analysis

PTEN Sequence Analysis

Baylor Genetics
United States
81
  • C Sequence analysis of the entire coding region

PTEN Deletion/Duplication Analysis (Prenatal Diagnosis)

Baylor Genetics
United States
81
  • D Deletion/duplication analysis

Results: 1 to 20 of 78

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.