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Results: 1 to 6 of 6

Tests names and labsConditionsGenes, analytes, and microbesMethods

Long QT syndrome (WES based NGS panel of 18 genes, including CNV analysis)

CGC Genetics Unilabs
Portugal
118
  • C Sequence analysis of the entire coding region

Cardiac conduction changes (WES based NGS panel of 29 genes, including CNV analysis)

CGC Genetics Unilabs
Portugal
129
  • C Sequence analysis of the entire coding region

SUDDEN DEATH/ IDIOPATHIC VENTRICULAR FIBRILLATION EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
1394
  • E Sequence analysis of select exons

HEREDITARY ARRHYTHMIA EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
1160
  • E Sequence analysis of select exons

Long QT Syndrome: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
1916
  • C Sequence analysis of the entire coding region

ALG10B Single Gene

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 6 of 6

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.