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Results: 21 to 40 of 57

Tests names and labsConditionsGenes, analytes, and microbesMethods

Invitae Arrhythmia and Cardiomyopathy Comprehensive Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
239100
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Arrhythmia Comprehensive Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
11541
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Cardiac Arrhythmia Panel

PreventionGenetics, part of Exact Sciences
United States
7965
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Brugada Syndrome Panel

PreventionGenetics, part of Exact Sciences
United States
917
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Left Ventricular Noncompaction (LVNC) Panel

PreventionGenetics, part of Exact Sciences
United States
1513
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Sick Sinus Syndrome and Brugada Syndrome via the HCN4 Gene

PreventionGenetics, part of Exact Sciences
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Brugada syndrome 8 (sequence analysis of HCN4 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 panel. NGS panel of 55 genes.

Genologica Medica
Spain
12855
  • C Sequence analysis of the entire coding region

Atrial fibrillation panel. NGS panel of 19 genes.

Genologica Medica
Spain
5519
  • C Sequence analysis of the entire coding region

Brugada syndrome panel. 9-gene NGS panel.

Genologica Medica
Spain
269
  • C Sequence analysis of the entire coding region

Brugada Syndrome Panel

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
2514
  • 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

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

Brugada Syndrome: gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
119
  • C Sequence analysis of the entire coding region

Brugada Syndrome NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
2618
  • C Sequence analysis of the entire coding region

Comprehensive Cardiac NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
174108
  • 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.