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Results: 1 to 20 of 102

Tests names and labsConditionsGenes and analytesMethods

CDKN1C sequencing

Genetic Services Laboratory University of Chicago
United States
21
  • C Sequence analysis of the entire coding region

Tempus xO assay

Tempus Labs, Inc.
United States
11714
  • R RNA analysis
  • C Sequence analysis of the entire coding region

IMAGE syndrome

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Metaphyseal dysplasia panel

Centogene AG - the Rare Disease Company
Germany
18
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beckwith-Wiedemann syndrome

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CDKN1C mutation analysis

Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam
Netherlands
21
  • C Sequence analysis of the entire coding region

Neonatal Diabetes Mellitus and Maturity-Onset Diabetes of the Young Deletion/Duplication Panel

Genetic Services Laboratory University of Chicago
United States
1141
  • D Deletion/duplication analysis

Tempus xT assay

Tempus Labs, Inc.
United States
2592
  • I Microsatellite instability testing (MSI)
  • R RNA analysis
  • C Sequence analysis of the entire coding region

CDKN1C. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

Beckwith-Wiedemann Syndrome via the CDKN1C Gene

PreventionGenetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Neonatal Diabetes Mellitus and Maturity-Onset Diabetes of the Young Panel

Genetic Services Laboratory University of Chicago
United States
1141
  • C Sequence analysis of the entire coding region

Hereditary Cancer Syndrome: Deletion/Duplication Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
11655
  • D Deletion/duplication analysis

Renal Cancer: Gene Deletion/Duplication Panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
122
  • D Deletion/duplication analysis

Renal Cancer: Gene Sequencing Panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
123
  • C Sequence analysis of the entire coding region

Wilms Tumor: Gene Deletion/Duplication Panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
32
  • D Deletion/duplication analysis

Wilms Tumor: Sequencing Panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
32
  • C Sequence analysis of the entire coding region

Hereditary Cancer Syndrome: Gene Deletion/Duplication Panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
155
  • D Deletion/duplication analysis

Hereditary Cancer Syndrome: Gene Sequencing Panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
160
  • C Sequence analysis of the entire coding region

IMAGe Syndrome: gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
21
  • C Sequence analysis of the entire coding region

Hereditary Sarcoma (Susceptibility to) , Panel Massive Sequencing (NGS) 25 Genes

Reference Laboratory Genetics
Spain
3325
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 102

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.

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