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Results: 81 to 100 of 100

Tests names and labsConditionsGenes, analytes, and microbesMethods

Hereditary Multiple Osteochondromas: gene deletion/duplication panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
12
  • D Deletion/duplication analysis

Comprehensive Skeletal Dysplasias and Disorders Panel

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

OSTEOCHONDROMA

Laboratorio de Genetica Clinica SL
Spain
12
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MULTIPLE EXOSTOSES (MULTIPLE OSTEOCHONDROMAS)

Laboratorio de Genetica Clinica SL
Spain
22
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Hereditary Multiple Osteochondromas Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
42
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Hereditary Cancer Panel

Blueprint Genetics
Finland
14146
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Cancer Syndromes - panels

MGZ Medical Genetics Center
Germany
6100
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Full Comprehensive Cancer Panel

Fulgent Genetics
United States
1166141
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Hereditary Cancer Panel

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
128130
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hemato-oncology chromosomal microarray

Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center
United States
2393
  • D Deletion/duplication analysis
  • H Detection of homozygosity

Multiple cartilaginous exostoses type 2

Bioarray
Spain
11
  • D Deletion/duplication analysis

Single gene testing EXT2

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

Hereditary multiple osteochondromas, EXT2 sequencing

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

EXT2 Sequencing

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

EXT2 Single Gene

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

Hereditary Multiple Osteochondromas (HM Exostoses) NGS Panel

Fulgent Genetics
United States
32
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Skeletal Dysplasias NGS Panel

Fulgent Genetics
United States
543178
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Multiple Osteochrondomas

Genetics Laboratory University of Oklahoma Health Sciences Center
United States
12
  • C Sequence analysis of the entire coding region

EXT2

Department of Medical Genetics - Wuyts Lab Antwerp University Hospital
Belgium
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 81 to 100 of 100

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.