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Results: 1 to 20 of 150

Tests names and labsConditionsGenes, analytes, and microbesMethods

Maturity-onset Diabetes of the Young Panel

Genetic Diagnostic Laboratory University of Pennsylvania School of Medicine
United States
1415
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neonatal Diabetes Panel

Genetic Services Laboratory University of Chicago
United States
317
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MODY Panel

Genetic Services Laboratory University of Chicago
United States
1015
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hyperinsulinism Panel

Genetic Services Laboratory University of Chicago
United States
1324
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

KCNJ11 Gene Diabetes mellitus, noninsulin-dependent NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

KCNJ11 Gene Hyperinsulinemic hypoglycemia type 2 NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

DiabetesNow Comprehensive Genetic Panel

GoPath Diagnostics
United States
115
  • D Deletion/duplication analysis

Tier 1 Panel: Diazoxide Unresponsive Hyperinsulinism

Genetic Services Laboratory University of Chicago
United States
23
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

KCNJ11

Department of Clinical Genetics Odense University Hospital
Denmark
21
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

GenepoweRx_Diabetes Care

GenepoweRx Uppaluri K&H Personalized Medicine Clinic
India
1741
  • D Deletion/duplication analysis
  • H Detection of homozygosity
  • S Mutation scanning of the entire coding region
  • T Targeted variant analysis

CentoScreen

Centogene AG - the Rare Disease Company
Germany
316314
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

KCNJ11 - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
51
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CentoIEM Panel

Centogene AG - the Rare Disease Company
Germany
669688
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Diabetes and Obesity Panel

Centogene AG - the Rare Disease Company
Germany
247262
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

CentoICU Panel

Centogene AG - the Rare Disease Company
Germany
829848
  • C Sequence analysis of the entire coding region

PGx-Premium (Preemptive PGx test)

SPMED CO., LTD Step forward Personalized Medicine
South Korea
6627
  • T Targeted variant analysis

Invitae Hypoglycemia Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
173119
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MODY and Neonatal Diabetes Panel, Sequencing

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
1723
  • C Sequence analysis of the entire coding region

Invitae Monogenic Diabetes Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
5928
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Monogenic Diabetes Panel

PreventionGenetics, part of Exact Sciences
United States
10154
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Results: 1 to 20 of 150

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.