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Results: 1 to 20 of 1515

Tests names and labsConditionsGenes, analytes, and microbesMethods

CEN4GEN comprehensive pharmacogenomic / pharmacogenetic screen

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
17
  • C Sequence analysis of the entire coding region

CEN4GEN cancer precision / cancer treatment / cancer pharmacogenetic / cancer pharmacogenomic screen

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • C Sequence analysis of the entire coding region

Prenatal cytogenetic testing of products of conception: SNP arrays

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • D Deletion/duplication analysis
  • U Uniparental disomy study (UPD)

Prenatal molecular cytogenetic: SNP arrays

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • D Deletion/duplication analysis
  • U Uniparental disomy study (UPD)

Prenatal molecular cytogenetics: CGH arrays

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • D Deletion/duplication analysis

Female infertility genetic testing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
16
  • K Karyotyping
  • I Microsatellite instability testing (MSI)
  • C Sequence analysis of the entire coding region

Male infertility genetic testing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
15
  • K Karyotyping
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Molecular cytogenetic: SNP arrays

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • D Deletion/duplication analysis
  • U Uniparental disomy study (UPD)

Molecular cytogenetic: CGH array

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • D Deletion/duplication analysis

Chromosomal microarray: hematological disorders and malignancies

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • D Deletion/duplication analysis

MUTYH-Associated Polyposis: MUTYH Common Mutation Panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • T Targeted variant analysis

Pan-Ethnic Carrier Screen: Full Gene Sequencing and SMA Analysis

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
1136
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypochondroplasia: targeted gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • C Sequence analysis of the entire coding region

Hand-Foot-Genital Syndrome: gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • C Sequence analysis of the entire coding region

Hereditary Motor and Sensory Neuropathy with Agenesis of the Corpus Callosum: targeted gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • T Targeted variant analysis

Hutchinson-Gilford Progeria Syndrome: targeted gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • T Targeted variant analysis

Myostatin-Related Muscle Hypertrophy: targeted gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • T Targeted variant analysis

HFE-Associated Hereditary Hemochromatosis: targeted gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • T Targeted variant analysis

X-Linked Dystonia-Parkinsonism (XPD) haplotyping: TAF1/DYT3 targeted gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • T Targeted variant analysis

Maple Syrup Urine Disease (Biochemical genetic testing)

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
14
  • A Analyte

Results: 1 to 20 of 1515

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.