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Results: 1 to 20 of 92

Tests names and labsConditionsGenes and analytesMethods

Long QT syndrome type 3

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

SCN5A Gene Sequencing

GENETIX Centro de Investigación en Genética Humana y Reproductiva
Colombia
41
  • S Mutation scanning of the entire coding region

SCN5A mutation analysis

Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam
Netherlands
61
  • C Sequence analysis of the entire coding region

Progressive familial heart block type I Deletion / Duplication panel

Connective Tissue Gene Tests
United States
92
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Progressive familial heart block type I Comprehensive panel

Connective Tissue Gene Tests
United States
92
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Progressive familial heart block type I NGS panel

Connective Tissue Gene Tests
United States
92
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Long QT syndrome Deletion / Duplication panel

Connective Tissue Gene Tests
United States
2619
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Long QT syndrome NGS panel

Connective Tissue Gene Tests
United States
2619
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Long QT syndrome Comprehensive panel

Connective Tissue Gene Tests
United States
2619
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

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

Fetal Concerns Sequencing Panel Sequencing Panel with CNV Detection

PreventionGenetics
United States
3840
  • D Deletion/duplication analysis
  • 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

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

Long QT Syndrome Sequencing Panel

PreventionGenetics
United States
1515
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

ANK2. Complete sequencing

Instituto de Medicina Genomica
Spain
41
  • C Sequence analysis of the entire coding region

KCNH2. MLPA testing

Instituto de Medicina Genomica
Spain
41
  • D Deletion/duplication analysis

Arrythmogenic Cardiomyopathy Panel

Health in Code
Spain
5517
  • C Sequence analysis of the entire coding region

KCNQ1. Complete sequencing

Instituto de Medicina Genomica
Spain
41
  • C Sequence analysis of the entire coding region

KCNH2, KCNQ1, SCN5A. NextGeneDx.Complete sequencing by NGS

Instituto de Medicina Genomica
Spain
33
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 92

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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