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Results: 1 to 20 of 35

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

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

CEN4GEN Targeted Medical exome: clinical exome sequencing (Proband only)

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

CEN4GEN Targeted Medical exome: clinical exome sequencing (Family Trios)

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

CEN4GEN Targeted Medical exome: clinical exome sequencing (Additional Family Member)

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

CEN4GEN Medical Whole Genome: Clinical Whole Genome, Proband Only

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

CEN4GEN Medical Whole Genome: Clinical Whole Genome, interpretation only

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

CEN4GEN Medical Whole Genome: Clinical Whole Genome, Family Trios

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

CEN4GEN Medical Whole Genome: Clinical Whole Genome, Additional Family Member

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

CEN4GEN Medical Whole Genome: Clinical Whole Genome re-analysis

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

CEN4GEN Medical Exome Array: Deletion/Duplication Analysis

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

CEN4GEN clinical whole exome: Reanalysis only

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

Results: 1 to 20 of 35

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.