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Results: 1 to 20 of 35

Tests names and labsConditionsGenes and analytesMethods

Expanded RASopathy Panel (14 Genes)

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
2014
  • 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

BRAF -Related Disorders via the BRAF Gene

PreventionGenetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Cardio-Facio-Cutaneous Syndrome Sanger Sequencing Panel

PreventionGenetics
United States
65
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Invitae Congenital Heart Disease not including Ciliopathies Panel

Invitae
United States
6640
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Epilepsy NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
3053447
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Prenatal Noonan Syndrome and Related Conditions Panel

Integrated Genetics Westborough Integrated Genetics
United States
49
  • C Sequence analysis of the entire coding region

BRAF Gene Sequencing

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
41
  • C Sequence analysis of the entire coding region

devSEEKĀ® - Noonan Syndrome/RASopathies Sequence Analysis

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
713
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Noonan Syndrome and related disorders (RASopathies) Panel

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
3011
  • C Sequence analysis of the entire coding region

Noonan Syndrome Panel

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
269
  • C Sequence analysis of the entire coding region

Cardiofaciocutaneous Syndrome Panel

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
124
  • C Sequence analysis of the entire coding region

Basal ganglia calcification Panel

CeGaT GmbH
Germany
5331
  • C Sequence analysis of the entire coding region

BRAF

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypertrophic Cardiomyopathy NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
15063
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cardio-Facio-Cutaneous Syndrome NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
155
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae RASopathies Comprehensive Panel

Invitae
United States
2616
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Cardio-Facio-Cutaneous Syndrome Panel

Invitae
United States
66
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

KRAS Full Gene Analysis

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
91
  • C Sequence analysis of the entire coding region

BRAF Full Gene Sequencing

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
71
  • S Mutation scanning of the entire coding region

Results: 1 to 20 of 35

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.