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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Micromelic Dysplasia NGS Panel Fulgent Genetics United States | 140 | 24 |
|
Microcephaly-Capillary Malformation Syndrome (STAMBP Single Gene Test) Fulgent Genetics United States | 32 | 1 |
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Retinopathy and Optic Atrophy NGS Panel Fulgent Genetics United States | 563 | 241 |
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Fulgent Genetics United States | 505 | 132 |
|
Fulgent Genetics United States | 85 | 7 |
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CHOPS Syndrome (AFF4 Single Gene Test) Fulgent Genetics United States | 27 | 1 |
|
Facial Dysostosis and Related Disorders NGS Panel Fulgent Genetics United States | 85 | 29 |
|
Fulgent Genetics United States | 121 | 23 |
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Comprehensive Primary Immunodeficiency NGS Panel Fulgent Genetics United States | 1048 | 472 |
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Comprehensive Cardiomyopathy NGS Panel Fulgent Genetics United States | 450 | 128 |
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Noonan and RASopathies NGS Panel Fulgent Genetics United States | 235 | 26 |
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Short Rib Dysplasia / Asphyxiating Thoracic Dysplasia NGS Panel Fulgent Genetics United States | 188 | 15 |
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Adams-Oliver Syndrome NGS Panel Fulgent Genetics United States | 55 | 6 |
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Fulgent Genetics United States | 76 | 5 |
|
Fulgent Genetics United States | 45 | 2 |
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Roberts Syndrome (ESCO2 Single Gene Test) Fulgent Genetics United States | 96 | 1 |
|
Fulgent Genetics United States | 339 | 61 |
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Fulgent Genetics United States | 533 | 149 |
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Congenital Heart Defect NGS Panel Fulgent Genetics United States | 377 | 114 |
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Beacon Expanded Female Carrier Screening Plus Panel Fulgent Genetics United States | 716 | 335 |
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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.