Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
22q11 microdeletion syndrome - FISH analysis GENETIX Centro de Investigación en Genética Humana y Reproductiva Colombia | 4 | 3 |
|
High-Resolution Rapid Microarray (CGH and SNP) Allele Diagnostics United States | 247 | 231 |
|
aCGH study for cryptic quantitative genomic imbalances Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 90 | 24 |
|
Rapid microarray (CGH and SNP) Allele Diagnostics United States | 247 | 231 |
|
Centogene US, LLC - The Rare Disease Company United States | 4 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 4 | 1 |
|
Invitae Leukodystrophy and Genetic Leukoencephalopathy Panel Invitae United States | 971 | 680 |
|
Invitae Inborn Errors of Immunity and Cytopenias Panel Invitae United States | 755 | 562 |
|
Invitae Hypoparathyroidism Panel Invitae United States | 41 | 18 |
|
SNP Microarray Analysis (Chromosomal Microarray) Institute for Genomic Medicine (IGM) Clinical Laboratory Nationwide Children's Hospital United States | 455 | 1 |
|
Congenital Anomalies of the Gastrointestinal Tract Panel PreventionGenetics United States | 297 | 180 |
|
VACTERL Association and Related Disorders Panel PreventionGenetics United States | 123 | 84 |
|
Nonsyndromic Congenital Heart Disease Panel PreventionGenetics United States | 54 | 44 |
|
Polydactyly and Syndactyly Panel PreventionGenetics United States | 320 | 231 |
|
Velocardiofacial syndrome, 192430, Autosomal dominant (22q11.2 deletion syndrome) (FISH) Intergen Genetic Diagnosis and Research Centre Turkey | 1 | 1 |
|
Velocardiofacial syndrome, 192430, Autosomal dominant (22q11.2 deletion syndrome) (Prenatal) (MLPA) Intergen Genetic Diagnosis and Research Centre Turkey | 1 | 1 |
|
Velocardiofacial syndrome, 192430, Autosomal dominant (22q11.2 deletion syndrome) (Prenatal) (FISH) Intergen Genetic Diagnosis and Research Centre Turkey | 1 | 1 |
|
Velocardiofacial syndrome, 192430, Autosomal dominant (22q11.2 deletion syndrome) (MLPA) Intergen Genetic Diagnosis and Research Centre Turkey | 1 | 1 |
|
PreventionGenetics United States | 220 | 128 |
|
Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins Hospital United States | 36 | 9 |
|
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