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Results: 21 to 40 of 57

Tests names and labsConditionsGenes, analytes, and microbesMethods

Cardiac Arrhythmia Exome Panel

Northwest Clinical Genomics Laboratory University Of Washington
United States
3951
  • C Sequence analysis of the entire coding region

Familial Atrial Fibrillation Syndrome Panel

PreventionGenetics, part of Exact Sciences
United States
1620
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Comprehensive Cardiac Arrhythmia Panel

PreventionGenetics, part of Exact Sciences
United States
7764
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Long QT Syndrome via the SCN4B Gene

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

SCN4B gene sequencing

Health in Code
Spain
11
  • C Sequence analysis of the entire coding region

Long QT syndrome 10 (sequence analysis of SCN4B gene)

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

Inherited Cadiac Disorders Panel

Dhiti Omics Technologies Private Ltd
India
6033
  • C Sequence analysis of the entire coding region

Arrhythmia & Cardiomyopathy Panel, Comprehensive

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
21193
  • C Sequence analysis of the entire coding region

Arrhythmia Panel, Comprehensive

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
7136
  • C Sequence analysis of the entire coding region

Long QT Syndrome Panel

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
3415
  • C Sequence analysis of the entire coding region

SCN4B

Institute for Human Genetics University Medical Center Freiburg
Germany
11
  • C Sequence analysis of the entire coding region

Familial Atrial fibrillation: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
1614
  • C Sequence analysis of the entire coding region

Comprehensive Cardiomyopathy NGS Panel

Fulgent Genetics
United States
450128
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Long QT/Brugada Syndrome NGS Panel

Fulgent Genetics
United States
6934
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Arrhythmogenic Right Ventricular Cardiomyopathy NGS Panel

Fulgent Genetics
United States
11846
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Long QT Syndrome: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
1916
  • C Sequence analysis of the entire coding region

Cardiology Genetic Panel (Full) , Panel Massive Sequencing (NGS) 96 Genes

Reference Laboratory Genetics
Spain
11995
  • C Sequence analysis of the entire coding region

Ventricular Arrhythmia and Sudden Cardiac Death , Panel Massive Sequencing (NGS) 48 Genes

Reference Laboratory Genetics
Spain
8148
  • C Sequence analysis of the entire coding region

Familial Atrial Fibrillation , Panel Massive Sequencing (NGS) 13 Genes

Reference Laboratory Genetics
Spain
1313
  • C Sequence analysis of the entire coding region

Long QT Syndrome , Panel Massive Sequencing (NGS) 11 Genes

Reference Laboratory Genetics
Spain
1111
  • C Sequence analysis of the entire coding region

Results: 21 to 40 of 57

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.