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Results: 1 to 20 of 51 (representing 27 labs)

Tests names and labsConditionsGenes and analytesMethods

Arrhythmogenic right ventricular cardiomyopathy type 11

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Pan Cardiomyopathy Panel (62 Genes)

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
10361
  • 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
9853
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Pan Cardiomyopathy Sequencing Panel

PreventionGenetics
United States
8882
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Dilated Cardiomyopathy Sequencing Panel

PreventionGenetics
United States
5147
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Sudden Cardiac Arrest Sequencing Panel

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

Comprehensive Cardiology Sequencing Panel

PreventionGenetics
United States
190164
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Comprehensive Cardiac Arrhythmia Sequencing Panel

PreventionGenetics
United States
6855
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Arrythmogenic Cardiomyopathy Panel

Health in Code S.L.
Spain
5517
  • C Sequence analysis of the entire coding region

DSC2, DSG2, DSP, JUP, PKP2, RYR2 (30 exones), TGFB3. NextGeneDx.Complete sequencing by NGS

Instituto de Medicina Genomica
Spain
77
  • C Sequence analysis of the entire coding region

Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia Sequencing Panel

PreventionGenetics
United States
89
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia via the DSC2 Gene

PreventionGenetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Arrhythmogenic Right Ventricular Dysplasia 11 - DSC2 Sequencing

Children's Hospital Colorado Molecular Genetics Laboratory Children's Hospital Colorado
United States
11
  • C Sequence analysis of the entire coding region

Arrhythmogenic right ventricular dysplasia - dominat (ARVD, deletion/duplication analysis of PKP2, DSP, JUP, DSC2, DSG2, TGFB3, RYR2 genes)

CGC Genetics
Portugal
77
  • D Deletion/duplication analysis

Arrhythmogenic right ventricular dysplasia - dominat (ARVD, deletion/duplication analysis of PKP2, DSP, JUP, DSC2, DSG2, TGFB3, RYR2 genes)

CGC Genetics
Portugal
77
  • D Deletion/duplication analysis

Comprehensive Cardiac Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
174107
  • C Sequence analysis of the entire coding region

FAMILIAL ISOLATED ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA

Laboratorio de Genetica Clinica SL
Spain
88
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Arrhythmogenic Right Ventricle Dysplasia Type 11 , Sequencing DSC2 Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Panel (ARVD/ARVC Panel)

Labor Dr. Wisplinghoff
Germany
2011
  • C Sequence analysis of the entire coding region

Invitae Cardiomyopathy and Skeletal Muscle Disease Panel

Invitae
United States
167113
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 51

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.

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