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Results: 61 to 77 of 77

Tests names and labsConditionsGenes, analytes, and microbesMethods

Comprehensive Skeletal Dysplasias and Disorders Panel

Blueprint Genetics
Finland
1246
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Mental retardation - different panels

Institute of Human Genetics Cologne University
Germany
72536
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Progressive Ossificans Fibrodysplasia, Sequencing ACVR1 Gene

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

Glaucoma

Asper Biogene Asper Biogene LLC
Estonia
1920
  • C Sequence analysis of the entire coding region

Congenital Structural Heart Disease Panel

Blueprint Genetics
Finland
962
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Solid Tumor Panel

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
2240
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Fibrodysplasia ossificans progressiva

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

Connective Tissue Disorders NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
3435
  • C Sequence analysis of the entire coding region

Congenital and Distal Myopathies Panel

CeGaT GmbH
Germany
4973
  • C Sequence analysis of the entire coding region

Fibrodysplasia ossificans progressiva(FOP),ACVR1 ,R206H sequencing

Molecular Diagnostics Laboratory Seoul National University Hospital
South Korea
11
  • E Sequence analysis of select exons

Fibrodysplasia ossificans progressiva(FOP), ACVR1 sequencing

Molecular Diagnostics Laboratory Seoul National University Hospital
South Korea
11
  • C Sequence analysis of the entire coding region

ACVR1 Single Gene

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

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Glaucoma NGS Panel

Fulgent Genetics
United States
6826
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Eye Disorders NGS Panel

Fulgent Genetics
United States
1018459
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Fibrodysplasia ossificans progressiva

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
11
  • C Sequence analysis of the entire coding region

Fibrodysplasia Ossificans Progressiva

Genetic Diagnostic Laboratory University of Pennsylvania School of Medicine
United States
11
  • T Targeted variant analysis

Results: 61 to 77 of 77

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.