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Results: 1 to 20 of 23

Tests names and labsConditionsGenes, analytes, and microbesMethods

Multiple Endoctine Neoplasia Type 2 (RET)

Molecular Genetics Laboratory London Health Sciences Centre
Canada
51
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

myRisk Hereditary Cancer

Myriad Genetics, Inc.
United States
3246
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

VistaSeq RET Comprehensive

Molecular Diagnostic Laboratory LabCorp
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Pheochromocytoma and Paraganglioma Panel

Genetic Services Laboratory University of Chicago
United States
1016
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

VistaSeq Comprehensive Cancer Panel

Molecular Diagnostic Laboratory LabCorp
United States
4759
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Endocrine Cancer Panel (12 Genes)

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
612
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Hereditary Cancer Panel (66 Genes)

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
3566
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Multiple Endocrine Neoplasia Type 2: RET Gene Deletion/Duplication

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

Endocrine tumours

Institute of Human Genetics Cologne University
Germany
1711
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Thyroid Cancer Panel

Genetic Services Laboratory University of Chicago
United States
1113
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Pediatric Solid Tumors Panel

Invitae
United States
9048
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Hereditary Cancer Panel

Genetic Services Laboratory University of Chicago
United States
25139
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Thyroid Cancer Panel

Invitae
United States
237
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Hyperparathyroidism Panel

Invitae
United States
95
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Multi-Cancer Panel

Invitae
United States
13980
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Multiple Endocrine Neoplasia Type 2 Test

Invitae
United States
61
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

RET Gene Sequencing and Deletion/Duplication Analysis

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
81
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Cancer Panel, Sequencing and Deletion/Duplication

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
3373
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

RET Sequencing and Deletion/Duplication

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Multiple Endocrine Neoplasia Type 2

MGZ Medical Genetics Center
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 23

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.