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Results: 1 to 20 of 20
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Centogene AG - the Rare Disease Company Germany | 218 | 135 |
|
SETD2 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
|
Centogene AG - the Rare Disease Company Germany | 777 | 770 |
|
Centogene AG - the Rare Disease Company Germany | 247 | 262 |
|
Invitae Monogenic Obesity Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 92 | 68 |
|
Invitae Overgrowth Syndromes Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 96 | 53 |
|
Autism Spectrum Disorders (ASD) Panel PreventionGenetics, part of Exact Sciences United States | 224 | 170 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Overgrowth and Macrocephaly Syndromes Panel PreventionGenetics, part of Exact Sciences United States | 145 | 112 |
|
Overgrowth syndrome Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 12 | 11 |
|
Overgrowth syndrome Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 12 | 11 |
|
HNL Genomics Connective Tissue Gene Tests United States | 12 | 11 |
|
Genetic Services Laboratory University of Chicago United States | 17 | 50 |
|
Macrocephaly / overgrowth syndrome panel. 43-gene NGS panel. Genologica Medica Spain | 88 | 43 |
|
Al Jalila Children’s Genomics Center Al Jalila Childrens Speciality Hospital United Arab Emirates | 38 | 40 |
|
Epilepsy Advanced Sequencing and CNV Evaluation - Intellectual Disability Athena Diagnostics United States | 57 | 56 |
|
Epilepsy Advanced Sequencing and CNV Evaluation Athena Diagnostics United States | 235 | 234 |
|
Invitae Overgrowth and Macrocephaly Syndromes Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 43 | 20 |
|
Results: 1 to 20 of 20
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.