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Results: 41 to 60 of 74

Tests names and labsConditionsGenes, analytes, and microbesMethods

Molecular profile of the tumor in melanoma. Panel NGS genes: BRAF, KIT, NRAS.

Genologica Medica
Spain
173
  • C Sequence analysis of the entire coding region

Hereditary leukemia panel. NGS panel of 39 genes.

Genologica Medica
Spain
8939
  • C Sequence analysis of the entire coding region

Noonan syndrome panel. NGS panel of 22 genes.

Genologica Medica
Spain
4822
  • C Sequence analysis of the entire coding region

Detection of somatic mutations in the NRAS gene

Genologica Medica
Spain
81
  • C Sequence analysis of the entire coding region

NRAS Mutations

Duzen Laboratories Duzen BBAGUAS
Turkey
41
  • T Targeted variant analysis

Arrhythmia & Cardiomyopathy Panel, Comprehensive

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
21193
  • C Sequence analysis of the entire coding region

Cardiomyopathy Panel, Comprehensive

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
17071
  • C Sequence analysis of the entire coding region

Cardiomyopathy Panel, Hypertrophic

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
8535
  • C Sequence analysis of the entire coding region

Cardiomyopathy Panel, Dilated

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
13448
  • C Sequence analysis of the entire coding region

Noonan Spectrum Disorders Panel

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
3613
  • C Sequence analysis of the entire coding region

Noonan syndrome

Al Jalila Children’s Genomics Center Al Jalila Childrens Speciality Hospital
United Arab Emirates
1818
  • C Sequence analysis of the entire coding region

NRAS

Institute for Human Genetics University Medical Center Freiburg
Germany
81
  • C Sequence analysis of the entire coding region

KRAS

Institute for Human Genetics University Medical Center Freiburg
Germany
121
  • C Sequence analysis of the entire coding region

Comprehensive Primary Immunodeficiency NGS Panel

Fulgent Genetics
United States
1048472
  • D Deletion/duplication analysis
  • 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

Noonan and RASopathies NGS Panel

Fulgent Genetics
United States
23526
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital Heart Defect NGS Panel

Fulgent Genetics
United States
377114
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

LYMPHOPROLIFERATIVE SYNDROME, AUTOIMMUNE

Laboratorio de Genetica Clinica SL
Spain
45
  • C Sequence analysis of the entire coding region

NRAS Single Gene

Fulgent Genetics
United States
1781
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hemolytic Anemia Panel by next-generation sequencing (NGS)

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
3334
  • E Sequence analysis of select exons

Results: 41 to 60 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.