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Results: 1 to 20 of 73

Tests names and labsConditionsGenes and analytesMethods

Brugada syndrome type 9

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

Brugada syndrome panel

Centogene AG - the Rare Disease Company
Germany
19
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Channelopathies

Cardiovascular Genetics PO San Francesco-NUORO (IT)
Italy
55
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cardiac Arrhythmia Gene Panel

Molecular Genetics Laboratory - Diagnostics Genetics LabPLUS - Auckland City Hospital
New Zealand
528
  • C Sequence analysis of the entire coding region

Brugada Syndrome via the SLMAP Gene

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

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

Brugada syndrome / J wave syndrome

Health in Code
Spain
125
  • C Sequence analysis of the entire coding region

Brugada Syndrome Gene Set

Genomics and Pathology Services Washington University in St. Louis
United States
211
  • C Sequence analysis of the entire coding region

Brugada Syndrome Panel

Health in Code
Spain
123
  • C Sequence analysis of the entire coding region

CardioGene Set

Genomics and Pathology Services Washington University in St. Louis
United States
980
  • C Sequence analysis of the entire coding region

Phosphorus Brugada Syndrome Panel

Phosphorus Diagnostics LLC
United States
110
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SCN3B Gene, entire coding region or targeted variant

Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute
Canada
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

SCN1B Gene, entire coding region or targeted variant

Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute
Canada
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

KCNE3 Gene, entire coding region or targeted variant

Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute
Canada
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

CACNA1C Gene, entire coding region or targeted variant

Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute
Canada
31
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

HCN4 Gene, entire coding region or targeted variant

Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute
Canada
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

KCNJ8 Gene, entire coding region or targeted variant

Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute
Canada
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

TRPM4 Gene, entire coding region or targeted variant

Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute
Canada
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

CACNA2D1 Gene, entire coding region or targeted variant

Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute
Canada
21
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Results: 1 to 20 of 73

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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