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Results: 1 to 15 of 15

Tests names and labsConditionsGenes, analytes, and microbesMethods

TECRL - NGS including CNV analysis

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

CentoCardio Panel

Centogene AG - the Rare Disease Company
Germany
289275
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Long QT Syndrome Panel

PreventionGenetics, Part of Exact Sciences
United States
2219
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Ventricular tachycardia, catecholaminergic polymorphic, 3, 614021, Autosomal recessive; CPVT3 (Catecholaminergic polymorphic ventricular tachycardia) (TECRL gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Comprehensive Cardiology Panel

PreventionGenetics, Part of Exact Sciences
United States
220196
  • 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

Catecholaminergic Polymorphic Ventricular Tachycardia Panel

PreventionGenetics, Part of Exact Sciences
United States
811
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

TECRL

Institute for Human Genetics University Medical Center Freiburg
Germany
11
  • 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

Long QT syndrome panel. 16-gene NGS panel.

Genologica Medica
Spain
3616
  • C Sequence analysis of the entire coding region

Catecholaminergic polymorphic ventricular tachycardia panel. 9-gene NGS panel.

Genologica Medica
Spain
129
  • C Sequence analysis of the entire coding region

Ventricular tachycardia, catecholaminergic polymorphic: Full gene sequencing panelc

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
55
  • C Sequence analysis of the entire coding region

Catecholminergic Polymorphic Ventricular Tachycardia (CPVT) Panel

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
1711
  • C Sequence analysis of the entire coding region

Cardiomyopathy and Arrhythmia Panel, Sequencing and Deletion/Duplication

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
12583
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Long QT Syndrome Panel

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
2519
  • C Sequence analysis of the entire coding region

Results: 1 to 15 of 15

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.