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Results: 1 to 20 of 26

Tests names and labsConditionsGenes, analytes, and microbesMethods

POMC - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Cholestasis Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
210134
  • D Deletion/duplication analysis

Invitae Hypoglycemia Panel

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

Invitae Monogenic Obesity Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
9268
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Obesity, adrenal insufficiency, and red hair due to POMC deficiency, 609734 (Obesity due to pro-opiomelanocortin deficiency) (POMC gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Obesity, adrenal insufficiency, and red hair due to POMC deficiency, 609734 (Obesity due to pro-opiomelanocortin deficiency) (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Comprehensive Monogenic Obesity Panel

PreventionGenetics, part of Exact Sciences
United States
4352
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Non-Syndromic Monogenic Obesity via the POMC Gene

PreventionGenetics, part of Exact Sciences
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Non-Syndromic Monogenic Obesity Panel

PreventionGenetics, part of Exact Sciences
United States
611
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Non-syndromic Monogenic Obesity Panel

Genetic Services Laboratory University of Chicago
United States
815
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

POMC Sequence Analysis (Familial Mutation/Variant Analysis)

Baylor Genetics
United States
21
  • T Targeted variant analysis

POMC Sequence Analysis

Baylor Genetics
United States
21
  • C Sequence analysis of the entire coding region

Monogenic obesity panel. 36-gene NGS panel.

Genologica Medica
Spain
5536
  • C Sequence analysis of the entire coding region

Glucocorticoid deficiency panel. 6-gene NGS panel.

Genologica Medica
Spain
76
  • C Sequence analysis of the entire coding region

Monogenic Obesity panel

Al Jalila Children’s Genomics Center Al Jalila Childrens Speciality Hospital
United Arab Emirates
3840
  • C Sequence analysis of the entire coding region

Proopiomelanocortin Deficiency (POMC Single Gene Test)

Fulgent Genetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Glucocorticoid Deficiency NGS Panel

Fulgent Genetics
United States
196
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Proopiomelanocortin Deficiency: gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • C Sequence analysis of the entire coding region

MONOGENIC OBESITY DUE TO MELANOCORTIN-LEPTIN PATHWAY DEFICIENCY

Laboratorio de Genetica Clinica SL
Spain
66
  • C Sequence analysis of the entire coding region

PROOPIOMELANOCORTIN (POMC)

MVZ Dr. Eberhard & Partner Dortmund
Germany
11
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 26

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.