Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Non-Syndromic Monogenic Obesity Panel PreventionGenetics, part of Exact Sciences United States | 6 | 11 |
|
Non-syndromic Monogenic Obesity Panel Genetic Services Laboratory University of Chicago United States | 8 | 15 |
|
Genetic Services Laboratory University of Chicago United States | 17 | 50 |
|
PCSK1 Sequence Analysis (Familial Mutation/Variant Analysis) Baylor Genetics United States | 2 | 1 |
|
Baylor Genetics United States | 2 | 1 |
|
Non syndromic obesity (WES based NGS panel of 22 genes, including analysis of CNVs) CGC Genetics Unilabs Portugal | 1 | 22 |
|
Obesity due to prohormone convertase I deficiency (sequence analysis of PCSK1 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
|
CONGENITAL DIARRHEA SYNDROME PANEL Laboratorio de Genetica Clinica SL Spain | 1 | 65 |
|
Monogenic obesity panel. 36-gene NGS panel. Genologica Medica Spain | 55 | 36 |
|
Genomic Unity® Custom Analysis Variantyx, Inc. United States | 1 | 4054 |
|
Genetic Services Laboratory University of Chicago United States | 10 | 93 |
|
Genetics Laboratory University of Oklahoma Health Sciences Center United States | 1 | 36 |
|
Carbohydrate Metabolism Deficiency (NGS Panel and Copy Number Analysis + mtDNA) MNG Laboratories (Medical Neurogenetics, LLC.) United States | 10 | 52 |
|
Prenatal Known Familial Mutation GeneDx United States | 1 | 1716 |
|
Custom XomeDxSlice (2-150 Genes, Proband Only) GeneDx United States | 1 | 1718 |
|
Al Jalila Children's Genomics Center Al Jalila Childrens Speciality Hospital United Arab Emirates | 38 | 40 |
|
Al Jalila Children's Genomics Center Al Jalila Childrens Speciality Hospital United Arab Emirates | 20 | 20 |
|
Kallmann Syndrome & Hypogonadotropic Hypogonadism NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States | 34 | 39 |
|
Hereditary kidney disorders - different panels Institute of Human Genetics Cologne University Germany | 32 | 481 |
|
MONOGENIC OBESITY DUE TO MELANOCORTIN-LEPTIN PATHWAY DEFICIENCY Laboratorio de Genetica Clinica SL Spain | 6 | 6 |
|
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