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Results: 1 to 20 of 55

Tests names and labsConditionsGenes and analytesMethods

Brugada syndrome type 5

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

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 SCN1B Gene

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

MECP2, SCN1B, GABRG2, LGI1, POLG, POLG2, SLC25A22, SPTAN1, SRPX2. NextGeneDx.Complete sequencing by NGS

Instituto de Medicina Genomica
Spain
209
  • C Sequence analysis of the entire coding region

nucSEEK® 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

Epilepsy and Seizure Disorders: Deletion/Duplication Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
164107
  • D Deletion/duplication analysis

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

BRUGADA SYNDROME

Laboratorio de Genetica Clinica SL
Spain
99
  • C Sequence analysis of the entire coding region

Fever Sensitive Seizures Spotlight Panel

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
2511
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Heart Diseases - panels

Medizinisch Genetisches Zentrum München MGZ München
Germany
4157
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SCN1B

Institute for Human Genetics University Clinic Freiburg
Germany
31
  • C Sequence analysis of the entire coding region

SCN1B Gene Sequencing

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
31
  • 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

Results: 1 to 20 of 55

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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