Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Syndromic Hearing Loss NGS Panel Fulgent Genetics United States | 223 | 83 |
|
Comprehensive Hearing Loss NGS Panel Fulgent Genetics United States | 332 | 167 |
|
Fulgent Genetics United States | 509 | 275 |
|
Roberts Syndrome (ESCO2 Single Gene Test) Fulgent Genetics United States | 96 | 1 |
|
Oxidative Phosphorylation Disorders NGS Panel Fulgent Genetics United States | 416 | 235 |
|
Hypomyelinating Leukodystrophy NGS Panel Fulgent Genetics United States | 225 | 62 |
|
Fulgent Genetics United States | 339 | 61 |
|
Coffin-Siris Syndrome NGS Panel Fulgent Genetics United States | 82 | 11 |
|
Beacon Expanded Female Carrier Screening Plus Panel Fulgent Genetics United States | 716 | 335 |
|
Beacon Expanded Male Carrier Screening Panel Fulgent Genetics United States | 636 | 298 |
|
Beacon Expanded Male Carrier Screening Plus Panel Fulgent Genetics United States | 661 | 306 |
|
Beacon Expanded Female Carrier Screening Panel Fulgent Genetics United States | 690 | 326 |
|
Fulgent Genetics United States | 16 | 1 |
|
Fulgent Genetics United States | 69 | 1 |
|
Fulgent Genetics United States | 26 | 1 |
|
Fulgent Genetics United States | 9 | 1 |
|
Fulgent Genetics United States | 75 | 1 |
|
Fulgent Genetics United States | 61 | 1 |
|
Fulgent Genetics United States | 96 | 1 |
|
Fulgent Genetics United States | 25 | 1 |
|
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.