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Results: 1 to 19 of 19

Tests names and labsConditionsGenes and analytesMethods

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

Comprehensive Familial Hyperinsulinism Panel

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

INSR

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

nucSEEK® Comprehensive Sequence Analysis Of The Nuclear Mitochondrial Exome

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
560420
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Endocrine Disorders: Deletion/Duplication Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
10857
  • D Deletion/duplication analysis

FAMILIAL HYPERINSULINEMIC HYPOGLYCEMIA (FAMILIAL HYPERINSULINISM)

Laboratorio de Genetica Clinica SL
Spain
55
  • C Sequence analysis of the entire coding region

Familial Hypoglycemia Hyperinsulinemia Type 5 , Sequencing INSR Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Abnormal Glucose/MODY Spotlight Panel

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
4931
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

INSR Gene Sequencing

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
31
  • C Sequence analysis of the entire coding region

Familial Hyperinsulinism NGS Panel

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
2610
  • C Sequence analysis of the entire coding region

FAMILIAR HYPERINSULINISM AND HYPERAMMONEMIA

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
1112
  • C Sequence analysis of the entire coding region

INSR

Fulgent Genetics
United States
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Endocrine Disorders: Sequencing Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
10857
  • C Sequence analysis of the entire coding region

Proportionate Short Stature/Small for Gestational Age: Sequencing and Deletion/Duplication Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
7745
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Nuclear-Mito NGS Panel

Fulgent Genetics
United States
601504
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MODY Neonatal Diabetes NGS Panel

Fulgent Genetics
United States
5530
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Intellectual Disability NGS Panel

Fulgent Genetics
United States
752392
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hyperinsulinism NGS Panel

Fulgent Genetics
United States
2711
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 19 of 19

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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