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Results: 21 to 36 of 36

Tests names and labsConditionsGenes, analytes, and microbesMethods

Hyperaldosteronism: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
44
  • C Sequence analysis of the entire coding region

Comprehensive Cardiomyopathy NGS Panel

Fulgent Genetics
United States
450128
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Long QT/Brugada Syndrome NGS Panel

Fulgent Genetics
United States
6934
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Arrhythmogenic Right Ventricular Cardiomyopathy NGS Panel

Fulgent Genetics
United States
11846
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Familial Hyperaldosteronism Type III , Sequencing KCNJ5 Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

KCNJ5 Gene Sequencing and Deletion/Duplication Analysis

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Single gene testing KCNJ5

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

Hyperaldosteronism, familial, type III

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

KCNJ5 Single Gene

Fulgent Genetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hyperaldosteronism

Institute of Human Genetics Cologne University
Germany
65
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Clinical Exome

Fulgent Genetics
United States
51294672
  • 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

Atrial Fibrillation NGS Panel

Fulgent Genetics
United States
6724
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Cardiovascular NGS Panel

Fulgent Genetics
United States
671250
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Arrhythmia NGS Panel

Fulgent Genetics
United States
18476
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hyperaldosteronism, familial, type III

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
11
  • S Mutation scanning of the entire coding region

Results: 21 to 36 of 36

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.