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Results: 1 to 20 of 53

Tests names and labsConditionsGenes and analytesMethods

Comprehensive Cardiac Arrhythmia NextGen Sequencing (NGS) Panel

PreventionGenetics
United States
5246
  • 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

KCNJ2. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

Andersen-Tawil Syndrome/Long QT Syndrome via the KCNJ2 Gene

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

TruGenome Predisposition Screen (Whole Genome Sequencing)

Illumina Clinical Services Laboratory Illumina
United States
15411578
  • C Sequence analysis of the entire coding region

nucSEEKĀ® Comprehensive Sequence Analysis Of The Nuclear Mitochondrial Exome

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
560420
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

KCNJ2 Sequencing

Heart Institute Diagnostic Lab Cincinnati Children's Hospital Medical Center
United States
11
  • S Mutation scanning of the entire coding region

Andersen Syndrome

Medical Genetics Laboratory Hallym University Hangang Sacred Heart Hospital
South Korea
11
  • C Sequence analysis of the entire coding region

Catecholaminergic Polymorphic Ventricular Tachycardia

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
77
  • C Sequence analysis of the entire coding region

Catecholaminergic polymorphic ventricular tachycardia

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
85
  • C Sequence analysis of the entire coding region

LONG QT SYNDROME

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
2023
  • C Sequence analysis of the entire coding region

Invitae Arrhythmia and Cardiomyopathy Comprehensive Panel

Invitae
United States
116119
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Arrhythmia Comprehensive Panel

Invitae
United States
6657
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Long QT syndrome type VII

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Andersen-Tawil syndrome (sequence analysis of KCNJ2 gene)

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

Single gene testing KCNJ2

CeGaT GmbH
Germany
31
  • C Sequence analysis of the entire coding region

Long QT syndrome (NGS panel for 14 genes)

CGC Genetics
Portugal
1314
  • C Sequence analysis of the entire coding region

Cardiac conduction changes (NGS panel for 27 genes)

CGC Genetics
Portugal
2627
  • C Sequence analysis of the entire coding region

Short QT Syndrome NGS Panel

DDC Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
146
  • C Sequence analysis of the entire coding region

Catecholaminergic Polymorphic Ventricular Tachycardia NGS Panel

DDC Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
96
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 53

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.