Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Invitae Neurotransmitter Disorders Panel Invitae United States | 52 | 44 |
|
Invitae Hereditary Hyperekplexia Panel Invitae United States | 23 | 13 |
|
Invitae United States | 466 | 297 |
|
X-Linked Intellectual Disability Panel PreventionGenetics, part of Exact Sciences United States | 191 | 141 |
|
Epilepsy: Early Infantile Epileptic Encephalopathy via the ARHGEF9 Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
|
Early Infantile Epileptic Encephalopathy Panel PreventionGenetics, part of Exact Sciences United States | 144 | 124 |
|
X-chromosome High Resolution microarray analysis Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center United States | 240 | 171 |
|
Non-Specific Intellectual Disability Panel Genetic Services Laboratory University of Chicago United States | 6 | 216 |
|
Early Infantile Epileptic Encephalopathy Panel Genetic Services Laboratory University of Chicago United States | 47 | 125 |
|
Institute for Human Genetics University Medical Center Freiburg Germany | 1 | 1 |
|
CGC Genetics Unilabs Portugal | 1 | 832 |
|
CGC Genetics Unilabs Portugal | 1 | 1293 |
|
Comprehensive Epilepsy Panel, Sequencing and Deletion/Duplication ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States | 234 | 240 |
|
Epileptic encephalopathy (WES based NGS panel of 137 genes, including CNV analysis) CGC Genetics Unilabs Portugal | 1 | 137 |
|
X-linked Intellectual Disability Panel CGC Genetics Unilabs Portugal | 1 | 104 |
|
Epileptic encephalopathy, early infantile type 8 (sequence analysis of ARHGEF9 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
|
Genomic Unity® X-Linked Intellectual Disability Plus Analysis Variantyx, Inc. United States | 1 | 108 |
|
Mendelics Brazil | 1 | 240 |
|
Neurodevelopmental and Movement Disorders Panel Mendelics Brazil | 2 | 121 |
|
X-LINKED INTELLECTUAL DISABILITY EXOME PANEL Laboratorio de Genetica Clinica SL Spain | 1 | 143 |
|
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.