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Results: 21 to 40 of 123

Tests names and labsConditionsGenes, analytes, and microbesMethods

CMNext®

Ambry Genetics
United States
13856
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CardioNext®

Ambry Genetics
United States
18992
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Pan Cardiomyopathy Panel

PreventionGenetics, part of Exact Sciences
United States
113106
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Dilated Cardiomyopathy Panel

PreventionGenetics, part of Exact Sciences
United States
6460
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hypertrophic Cardiomyopathy Panel

PreventionGenetics, part of Exact Sciences
United States
6660
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Sudden Cardiac Arrest Panel

PreventionGenetics, part of Exact Sciences
United States
6349
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Comprehensive Cardiology Panel

PreventionGenetics, part of Exact Sciences
United States
223198
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Invitae Congenital Heart Disease Panel

Invitae
United States
10755
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cardiac Arrhythmia Exome Panel

Northwest Clinical Genomics Laboratory University Of Washington
United States
3951
  • C Sequence analysis of the entire coding region

Cardiomyopathy Exome Panel

Northwest Clinical Genomics Laboratory University Of Washington
United States
3275
  • C Sequence analysis of the entire coding region

Comprehensive Cardiac Arrhythmia Panel

PreventionGenetics, part of Exact Sciences
United States
7764
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hypertrophic Cardiomyopathy panel

Clinical Genomics Laboratory Washington University in St. Louis
United States
142
  • C Sequence analysis of the entire coding region

Dilated Cardiomyopathy panel

Clinical Genomics Laboratory Washington University in St. Louis
United States
168
  • C Sequence analysis of the entire coding region

Cardiomyopathy panel

Clinical Genomics Laboratory Washington University in St. Louis
United States
596
  • C Sequence analysis of the entire coding region

Cardiac Diseases Gene panel

Clinical Genomics Laboratory Washington University in St. Louis
United States
12150
  • C Sequence analysis of the entire coding region

Hypertrophic Cardiomyopathy and Dilated Cardiomyopathy via the MYH6 Gene

PreventionGenetics, part of Exact Sciences
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Comprehensive Cardiomyopathy Panel (37 genes)

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
437
  • X Mutation scanning of select exons
  • S Mutation scanning of the entire coding region

MYH6

Institute for Human Genetics University Medical Center Freiburg
Germany
41
  • C Sequence analysis of the entire coding region

Hypertrophic cardiomyopathy (WES based NGS panel of 68 genes, including CNV analysis)

CGC Genetics Unilabs
Portugal
168
  • C Sequence analysis of the entire coding region

Dilated cardiomyopathy (WES based NGS panel of 81 genes, including CNV analysis)

CGC Genetics Unilabs
Portugal
181
  • C Sequence analysis of the entire coding region

Results: 21 to 40 of 123

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.