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Results: 1 to 20 of 86

Tests names and labsConditionsGenes, analytes, and microbesMethods

Comprehensive Arrhythmia Gene Panel

Mayo Clinic Laboratories Mayo Clinic
United States
3644
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Arrhythmogenic Cardiomyopathy Panel

Mayo Clinic Laboratories Mayo Clinic
United States
2618
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cardiomyopathy and Arrhythmia Panel

Mayo Clinic Laboratories Mayo Clinic
United States
73105
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Cardiomyopathy Panel

Mayo Clinic Laboratories Mayo Clinic
United States
6883
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypertrophic Cardiomyopathy Panel

Mayo Clinic Laboratories Mayo Clinic
United States
4448
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Dilated Cardiomyopathy/LVNC Panel

Mayo Clinic Laboratories Mayo Clinic
United States
5263
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CentoCardio Panel

Centogene AG - the Rare Disease Company
Germany
289275
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Heart Health Test

Color Diagnostics, LLC DBA Color Health
United States
1930
  • C Sequence analysis of the entire coding region

Targeted Cardiomyopathy panel

Molecular Cardiology Laboratories Istituti Clinici Scientifici Maugeri, IRCCS
Italy
441
  • S Mutation scanning 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

Invitae Hypertrophic Cardiomyopathy Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
7559
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SCO2 Sequencing

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
21
  • S Mutation scanning of the entire coding region

MYL3 Sequencing

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
11
  • S Mutation scanning of the entire coding region

MYH7 Sequencing

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
41
  • S Mutation scanning of the entire coding region

MYBPC3 Sequencing

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
41
  • S Mutation scanning of the entire coding region

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

Hereditary Disease Risk Test

Color Diagnostics, LLC DBA Color Health
United States
5159
  • C Sequence analysis of the entire coding region

Hypertrophic Cardiomyopathy Panel, Sequencing

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
2534
  • C Sequence analysis of the entire coding region

mtDNA Targeted Analysis: Known Familial Mutation

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
1134
  • T Targeted variant analysis

mtDNA Targeted Analysis with Heteroplasmy: Known Familial Mutation

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
1134
  • T Targeted variant analysis

Results: 1 to 20 of 86

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.