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Results: 41 to 53 of 53

Tests names and labsConditionsGenes, analytes, and microbesMethods

Stroke (NGS Panel and Copy Number Analysis + mtDNA)

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
385
  • C Sequence analysis of the entire coding region

Autism/ID Xpanded Panel

GeneDx
United States
22592
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Osteogenesis Imperfecta Panel

GeneDx
United States
124
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Osteogenesis imperfecta: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
1817
  • C Sequence analysis of the entire coding region

Osteogenesis Imperfecta and Decreased Bone Density NGS Panel

Fulgent Genetics
United States
11132
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Growth Disorders / Skeletal Dysplasias and Disorders Panel

Blueprint Genetics
Finland
2308
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Osteogenesis Imperfecta Panel

Blueprint Genetics
Finland
127
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SPARC Single Gene

Fulgent Genetics
United States
101
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Osteogenesis imperfecta and related skeletal dysplasias with decreased bone density panel

CeGaT GmbH
Germany
2327
  • C Sequence analysis of the entire coding region

Osteogenesis Imperfecta and Genetic Bone Disorders Panel

Collagen Diagnostic Laboratory University of Washington
United States
2730
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

OI panel 2

Connective Tissue Laboratory Ghent University Hospital
Belgium
119
  • C Sequence analysis of the entire coding region

Osteogenesis Imperfecta NGS Panel

Fulgent Genetics
United States
5714
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51304674
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 41 to 53 of 53

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.