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Results: 1 to 20 of 74

Tests names and labsConditionsGenes, analytes, and microbesMethods

NGS RASopathy Panel

Institute for Genomic Medicine (IGM) Clinical Laboratory Nationwide Children's Hospital
United States
914
  • C Sequence analysis of the entire coding region

Cardiomyopathy and Arrhythmia Panel

Mayo Clinic Laboratories Mayo Clinic
United States
73105
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Cardiomyopathy Panel

Mayo Clinic Laboratories Mayo Clinic
United States
6883
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital Heart Disease Gene Panel

Mayo Clinic Laboratories Mayo Clinic
United States
2244
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypertrophic Cardiomyopathy Panel

Mayo Clinic Laboratories Mayo Clinic
United States
4448
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Dilated Cardiomyopathy/LVNC Panel

Mayo Clinic Laboratories Mayo Clinic
United States
5263
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Noonan Syndrome and Related Panel

Mayo Clinic Laboratories Mayo Clinic
United States
1520
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Non-NF1 RASopathy NGS Panel

Medical Genomics Laboratory Department of Genetics UAB
United States
717
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

NOONAN SYNDROME

Clinical Genomics Unit Hospital Universitari Germans Trias i Pujol
Spain
516
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

RASOPATHY-RELATED SYNDROME

Clinical Genomics Unit Hospital Universitari Germans Trias i Pujol
Spain
919
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

CentoDysmorph Panel

Centogene AG - the Rare Disease Company
Germany
740728
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PGmax™ - Comprehensive Congenital Heart Disease Panel

PreventionGenetics, part of Exact Sciences
United States
241
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Noonan syndrome core NGS panel

HNL Genomics Connective Tissue Gene Tests
United States
1014
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Noonan syndrome core Comprehensive panel

HNL Genomics Connective Tissue Gene Tests
United States
1014
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Noonan syndrome core Deletion / Duplication panel

HNL Genomics Connective Tissue Gene Tests
United States
1014
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cardiomyopathy Exome Panel

Northwest Clinical Genomics Laboratory University Of Washington
United States
3275
  • C Sequence analysis of the entire coding region

Cardiac Diseases Gene panel

Clinical Genomics Laboratory Washington University in St. Louis
United States
12150
  • C Sequence analysis of the entire coding region

Noonan syndrome (sequence analysis of KRAS gene)

CGC Genetics Unilabs
Portugal
11
  • C Sequence analysis of the entire coding region

Noonan syndrome (sequence analysis of RIT1 gene)

CGC Genetics Unilabs
Portugal
11
  • C Sequence analysis of the entire coding region

Lymphedema

Genetic Diagnostic Laboratory University of Pennsylvania School of Medicine
United States
157
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 74

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.