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Results: 1 to 20 of 133

Tests names and labsConditionsGenes and analytesMethods

MODY Deletion/Duplication Panel

Genetic Services Laboratory University of Chicago
United States
1014
  • D Deletion/duplication analysis

Diabetes mellitus, noninsulin-dependent

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

CentoICU platinum

Centogene AG - the Rare Disease Company
Germany
769514
  • C Sequence analysis of the entire coding region

CentoICU platinum plus

Centogene AG - the Rare Disease Company
Germany
769514
  • C Sequence analysis of the entire coding region

MODY Panel

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

Diabetes mellitus noninsulin-dependent

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

ExomePLUS Cystic Disease & Dysplasia/Agenesis

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
2122
  • C Sequence analysis of the entire coding region

ExomePLUS Electrolyte & Kidney Stone

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
4649
  • C Sequence analysis of the entire coding region

HNF4,GCK,HNF1A,HNF1B, NextGeneDx.Complete sequencing by NGS

Instituto de Medicina Genomica
Spain
44
  • C Sequence analysis of the entire coding region

WFS1 Gene Sequencing 

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
61
  • C Sequence analysis of the entire coding region

MitoMet®Plus aCGH Analysis

Baylor Miraca Genetics Laboratories
United States
845637
  • D Deletion/duplication analysis

Hearing Loss: Deletion/Duplication Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
15991
  • D Deletion/duplication analysis

MODY Panel

Ambry Genetics
United States
145
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Familial Hypomagnesemia , Panel Massive Sequencing (NGS) 14 Genes

Reference Laboratory Genetics
Spain
1614
  • C Sequence analysis of the entire coding region

Hyperinsulinism-Hyperammonemia syndrome , Panel Massive Sequencing (NGS) 12 Genes

Reference Laboratory Genetics
Spain
1212
  • C Sequence analysis of the entire coding region

Permanent Neonatal Diabetes Mellitus , Panel Massive Sequencing (NGS) 16 Genes

Reference Laboratory Genetics
Spain
1216
  • C Sequence analysis of the entire coding region

Glycogen Storage Disease, Panel Massive Sequencing (NGS) 11 Genes

Reference Laboratory Genetics
Spain
1311
  • C Sequence analysis of the entire coding region

Diabetes MODY, Panel Massive Sequencing (NGS) 11 Genes

Reference Laboratory Genetics
Spain
1911
  • C Sequence analysis of the entire coding region

WFS1 Gene Sequencing

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
51
  • C Sequence analysis of the entire coding region

SLC2A2 Gene Sequencing

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
21
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 133

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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