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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
NGS Panel for Hemochromatosis and Hyperferritinemia /Hypoferritinemia Panel BloodGenetics Spain | 11 | 11 |
|
Invitae Leukodystrophy and Genetic Leukoencephalopathy Panel Invitae United States | 971 | 680 |
|
Invitae Supplemental Metabolic Newborn Screening Panel Invitae United States | 253 | 189 |
|
Non-Immune Hydrops Fetalis Panel PreventionGenetics, part of Exact Sciences United States | 291 | 148 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Inherited Glycosylphosphatidylinositol Biosynthesis Defects (IGDs) Panel PreventionGenetics, part of Exact Sciences United States | 23 | 21 |
|
Invitae Metabolic Non-Immune Fetal Hydrops Panel Invitae United States | 50 | 51 |
|
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 via the PIGA Gene PreventionGenetics, part of Exact Sciences United States | 2 | 1 |
|
Invitae United States | 466 | 297 |
|
Invitae Congenital Disorders of Glycosylation Panel Invitae United States | 203 | 152 |
|
X-Linked Intellectual Disability Panel PreventionGenetics, part of Exact Sciences United States | 191 | 141 |
|
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 |
|
Institute for Human Genetics University Medical Center Freiburg Germany | 3 | 1 |
|
Epileptic encephalopathy panel. 128-gene NGS panel. Genologica Medica Spain | 197 | 128 |
|
Macrocephaly / overgrowth syndrome panel. 43-gene NGS panel. Genologica Medica Spain | 88 | 43 |
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Plugin system clutter panel. NGS panel of 75 genes. Genologica Medica Spain | 76 | 75 |
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Complete epilepsy panel. NGS panel of 283 genes. Genologica Medica Spain | 409 | 283 |
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Congenital Disorders of Glycosylation Panel CNH Molecular Diagnostics Laboratory Childrens National Hospital United States | 51 | 41 |
|
Paroxysmal nocturnal hemoglobinuria: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 2 | 2 |
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