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Results: 1 to 13 of 13

Tests names and labsConditionsGenes, analytes, and microbesMethods

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 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 PGLNext® (+RNAinsight®)

Ambry Genetics
United States
261
  • 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
14118
  • D Deletion/duplication analysis
  • R RNA analysis
  • C Sequence analysis of the entire coding region

RenalNext®

Ambry Genetics
United States
5720
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PGLNext®

Ambry Genetics
United States
2614
  • D Deletion/duplication 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
14177
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Paraganglioma-Pheochromocytoma (PGL/PCC) Syndrome Panel

PreventionGenetics
United States
1313
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

SDHD

Division of Human Genetics Medical University Innsbruck
Austria
51
  • S Mutation scanning of the entire coding region
  • 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
4759
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Paraganglioma

Genetics Laboratory University of Oklahoma Health Sciences Center
United States
11
  • C Sequence analysis of the entire coding region

Results: 1 to 13 of 13

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.