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Results: 1 to 20 of 21

Tests names and labsConditionsGenes and analytesMethods

Pan Cardiomyopathy Panel (62 Genes)

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
10362
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

DCM/Arrhythmogenic Cardiomyopathy Panel (53 Genes)

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
9753
  • 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
4151
  • 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

Familial Atrial Fibrillation Syndrome NextGen Sequencing (NGS) Panel

PreventionGenetics
United States
1015
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Comprehensive Cardiac Arrhythmia NextGen Sequencing (NGS) Panel

PreventionGenetics
United States
5246
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Cantu Syndrome via the ABCC9 Gene

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

nucSEEK® Comprehensive Sequence Analysis Of The Nuclear Mitochondrial Exome

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
560420
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

ABCC9

Institute for Human Genetics University Clinic Freiburg
Germany
31
  • C Sequence analysis of the entire coding region

Atrial Fibrillation and Short QT Syndrome Panel

CeGaT GmbH
Germany
1117
  • C Sequence analysis of the entire coding region

Cardiomyopathy and Arrhythmia Panel, Sequencing (85 Genes) and Deletion/Duplication (83 Genes)

ARUP Laboratories, Molecular Genetics University of Utah ARUP Lab
United States
14785
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cardiomyopathy and Arrhythmia Panel, Sequencing, 85 Genes

ARUP Laboratories, Molecular Genetics University of Utah ARUP Lab
United States
14785
  • C Sequence analysis of the entire coding region

Cardio-channelopathy-gene-panel

MVZ Dortmund Dr. Eberhard and Partner
Germany
3533
  • C Sequence analysis of the entire coding region

ABCC9

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypertrophic Cardiomyopathy NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
15063
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Dilated Cardiomyopathy NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
8732
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cardiomyopathy: Sequencing and Deletion/Duplication Panel

Emory Genetics Laboratory Emory University
United States
230106
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Nuclear-Mito NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
601504
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cardiomyopathy panel

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
13461
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Atrial Fibrillation NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
7523
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 21

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.