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Results: 41 to 60 of 69

Tests names and labsConditionsGenes, analytes, and microbesMethods

Arrhythmia

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

Brugada Syndrome NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
2618
  • C Sequence analysis of the entire coding region

Comprehensive Cardiac NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
174108
  • 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

Heart Diseases - panels

MGZ Medical Genetics Center
Germany
4157
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SCN1B Gene Sequencing and Deletion/Duplication Analysis

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Epilepsy Comprehensive NGS Panel

Fulgent Genetics
United States
729398
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Brugada syndrome type V

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

Brugada Syndrome

Asper Biogene Asper Biogene LLC
Estonia
1111
  • C Sequence analysis of the entire coding region

Single gene testing SCN1B

CeGaT GmbH
Germany
21
  • C Sequence analysis of the entire coding region

Brugada Syndrome Panel

CeGaT GmbH
Germany
913
  • C Sequence analysis of the entire coding region

Cardio-channelopathy-gene-panel

MVZ Dr. Eberhard & Partner Dortmund
Germany
3533
  • C Sequence analysis of the entire coding region

Brugada Syndrome 5, Cardiac conduction defect, nonspecific, SCN1B

MVZ Dr. Eberhard & Partner Dortmund
Germany
11
  • C Sequence analysis of the entire coding region

SCN1B Single Gene

Fulgent Genetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Nuclear-Mito NGS Panel

Fulgent Genetics
United States
1103676
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Sudden Death Syndrome NGS Panel

Fulgent Genetics
United States
16868
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cardiac conduction abnormalities panel

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
7633
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Febrile seizures / genetic epilepsy with febrile seizures plus (GEFS+) panel

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
2210
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Epileptic encephalopathy panel

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
5332
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Results: 41 to 60 of 69

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.