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Results: 1 to 20 of 45

Tests names and labsConditionsGenes and analytesMethods

Brugada syndrome type 7

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

Sudden Cardiac Arrest Sequencing Panel with CNV Detection

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

Comprehensive Cardiology Sequencing Panel with CNV Detection

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

Brugada Syndrome Sequencing Panel

PreventionGenetics
United States
916
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Brugada Syndrome via the SCN3B Gene

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

RhythmFirst reflex RhythmNext

Ambry Genetics
United States
8736
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

RhythmNext

Ambry Genetics
United States
8736
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CustomNext: Cardio

Ambry Genetics
United States
238106
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CardioNext with TTN

Ambry Genetics
United States
19285
  • D Deletion/duplication analysis
  • 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

Brugada Syndrome, Panel Massive Sequencing (NGS) 8 Genes

Reference Laboratory Genetics
Spain
88
  • C Sequence analysis of the entire coding region

Brugada Syndrome: Deletion/Duplication Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
188
  • D Deletion/duplication analysis

Arrhythmias: Deletion/Duplication Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
6029
  • D Deletion/duplication analysis

Arrhythmia

Asper Biogene Asper Biogene LLC
Estonia
6638
  • C Sequence analysis of the entire coding region

BRUGADA SYNDROME/LONG-QT/SHORT-QT/VENTRICULAR TACHYCARDIA: NGS PANEL

Laboratorio de Genetica Clinica SL
Spain
2625
  • C Sequence analysis of the entire coding region

Brugada Syndrome Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
2616
  • C Sequence analysis of the entire coding region

Comprehensive Cardiac Panel

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

Results: 1 to 20 of 45

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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