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Results: 1 to 20 of 40 (representing 16 labs)

Tests names and labsConditionsGenes and analytesMethods

Arrhythmogenic right ventricular cardiomyopathy type 1

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

Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia via the TGFB3 Gene

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

Comprehensive Cardiac Arrhythmia Sequencing Panel

PreventionGenetics
United States
5246
  • 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

TGFBR1, TGFBR2, FBN1, ACTA2, FBN2, ELN, TGFBR3. NextGeneDx.Complete sequencing by NGS

Instituto de Medicina Genomica
Spain
77
  • 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

TGFB3

Institute for Human Genetics University Clinic Freiburg
Germany
21
  • C Sequence analysis of the entire coding region

Invitae Cardiomyopathy and Skeletal Muscle Disease Panel

Invitae
United States
190150
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

TGFB3 Gene Sequencing

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
21
  • C Sequence analysis of the entire coding region

CARDIOMYOPATHY, ARRHYTHMOGENIC RIGHT VENTRICULAR (ARVC)

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
109
  • C Sequence analysis of the entire coding region

Invitae Cardiomyopathy Comprehensive Panel

Invitae
United States
8179
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Arrhythmogenic Cardiomyopathy Panel

Invitae
United States
1223
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Arrhythmia and Cardiomyopathy Comprehensive Panel

Invitae
United States
127112
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Arrhythmia Comprehensive Panel

Invitae
United States
7362
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Loeys-Dietz syndrome 5 (LDS5) genomic sequencing and deletion/duplication analysis

Collagen Diagnostic Laboratory University of Washington
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Arrhythmogenic Right Ventricular Cardiomyopathy Panel

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
209
  • C Sequence analysis of the entire coding region

Arrhythmogenic right ventricular dysplasia 1 (sequence analysis of TGFB3 gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

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

CeGaT GmbH
Germany
1413
  • C Sequence analysis of the entire coding region

FBN1 mutational analysis

Connective Tissue Laboratory Ghent University Hospital
Belgium
191
  • E Sequence analysis of select exons

Results: 1 to 20 of 40

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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