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Results: 1 to 20 of 109

Tests names and labsConditionsGenes and analytesMethods

Otogenetics Hereditary Cancers

Otogenetics
United States
3639
  • E Sequence analysis of select exons

Multiple endocrine neoplasia type 1

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

Multiple Endoctine Neoplasia Type 1 (MENIN)

Molecular Genetics Laboratory London Health Sciences Centre
Canada
11
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Hyperparathyroidism Deletion/Duplication Panel

Genetic Services Laboratory University of Chicago
United States
68
  • D Deletion/duplication analysis

Genetic Test of single known genetic variant

National Taiwan University Hospital A1 Center National Taiwan University Hospital
Taiwan
710
  • E Sequence analysis of select exons

Multiple Endocrine Neoplasia,Type1(MEN1) Genetic Test

National Taiwan University Hospital A1 Center National Taiwan University Hospital
Taiwan
11
  • C Sequence analysis of the entire coding region

Hereditary Thyroid and Other Neuroendocrine Gland Cancer-Mutation

GeneKor MSA
Greece
11
  • C Sequence analysis of the entire coding region

Hereditary Pheochromocytoma and Paraganglioma Panel

Genetic Services Laboratory University of Chicago
United States
1014
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MEN1. MLPA testing

Instituto de Medicina Genomica
Spain
11
  • D Deletion/duplication analysis

MEN1. Complete sequencing

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

Cancer Sequencing Panel with CNV Detection

PreventionGenetics
United States
4131
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hereditary Paraganglioma-Pheochromocytoma Syndrome Sequencing Panel

PreventionGenetics
United States
1212
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

MitoMet®Plus aCGH Analysis

Baylor Miraca Genetics Laboratories
United States
844637
  • D Deletion/duplication analysis

Multiple Endocrine Neoplasia Type 1 via MEN1 Gene Sequencing with CNV Detection

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

Hereditary Cancer Syndrome: Deletion/Duplication Panel

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

PGLNext

Ambry Genetics
United States
2612
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MEN1 gene sequence and deletion/duplication

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

CustomNext: Cancer

Ambry Genetics
United States
14668
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CancerNext-Expanded

Ambry Genetics
United States
14164
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

BrainTumorNext

Ambry Genetics
United States
7227
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 109

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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