Filters
reset allOther countries
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Molecular Vision Laboratory United States | 1358 | 1028 |
|
LTBP2 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 3 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 417 | 413 |
|
PreventionGenetics, part of Exact Sciences United States | 285 | 137 |
|
Invitae Limb and Digital Malformations Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 356 | 177 |
|
Labcorp Genetics (formerly Invitae) LabCorp United States | 57 | 27 |
|
Lysosomal Storage Disorders Panel PreventionGenetics, part of Exact Sciences United States | 242 | 146 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Anterior Segment Dysgenesis Disorders Panel PreventionGenetics, part of Exact Sciences United States | 272 | 278 |
|
PreventionGenetics, part of Exact Sciences United States | 157 | 171 |
|
Connective tissue disorder NGS panel HNL Genomics Connective Tissue Gene Tests United States | 37 | 47 |
|
Connective tissue disorder Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 37 | 47 |
|
Connective tissue disorder Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 37 | 47 |
|
Weill-Marchesani syndrome Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 4 | 4 |
|
Weill-Marchesani syndrome Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 4 | 4 |
|
Weill-Marchesani syndrome NGS panel HNL Genomics Connective Tissue Gene Tests United States | 4 | 4 |
|
Comprehensive Cardiology Panel PreventionGenetics, part of Exact Sciences United States | 223 | 198 |
|
PreventionGenetics, part of Exact Sciences United States | 38 | 24 |
|
Central skeletal dysplasias panel. NGS panel of 111 genes. Genologica Medica Spain | 258 | 111 |
|
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.