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Results: 21 to 32 of 32

Tests names and labsConditionsGenes, analytes, and microbesMethods

Arrhythmia panel. NGS panel of 55 genes.

Genologica Medica
Spain
12855
  • C Sequence analysis of the entire coding region

Sudden cardiac failure, alcohol-induced: Full gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • C Sequence analysis of the entire coding region

Genomic Unity® Custom Analysis

Variantyx, Inc.
United States
14054
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

SCA Arrhythmia Panel

GeneDx
United States
514
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Mitochondrial genome sequencing

Molecular Vision Laboratory
United States
526339
  • C Sequence analysis of the entire coding region

Congenital Hypotonia Xpanded Panel

GeneDx
United States
101423
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Arrhythmia Sequencing and Del/Dup Panel

GeneDx
United States
558
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Combined Cardiac Sequencing and Del/Dup Panel

GeneDx
United States
10138
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cardiomyopathy Panel

Blueprint Genetics
Finland
6155
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Cardiology Panel

Blueprint Genetics
Finland
12185
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Arrhythmia Panel

Blueprint Genetics
Finland
755
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PPA2 Single Gene

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

Results: 21 to 32 of 32

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.