Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Invitae Broad Carrier Screen without X-linked Disorders Invitae United States | 195 | 98 |
|
Invitae United States | 224 | 112 |
|
Invitae Comprehensive Carrier Screen Invitae United States | 886 | 547 |
|
Glycogen Storage Disease Type 1b Myriad Genetics, Inc. United States | 1 | 1 |
|
Invitae Autoinflammatory and Autoimmunity Syndromes Panel Invitae United States | 223 | 154 |
|
Invitae Comprehensive Glycogen Storage Disease Panel Invitae United States | 37 | 28 |
|
Invitae Monogenic Inflammatory Bowel Disease Panel Invitae United States | 108 | 67 |
|
Invitae Primary Immunodeficiency Panel Invitae United States | 552 | 424 |
|
PreventionGenetics United States | 38 | 38 |
|
Invitae Congenital Disorders of Glycosylation Panel Invitae United States | 203 | 152 |
|
Invitae Bone Marrow Failure Syndromes Panel Invitae United States | 138 | 85 |
|
Severe Congenital Neutropenia Panel PreventionGenetics United States | 26 | 25 |
|
Glycogen Storage Disease and Disorders of Glucose Metabolism Panel PreventionGenetics United States | 33 | 33 |
|
SLC37A4 Comprehensive - Sequence & Deletion/Duplication Analysis Baylor Genetics United States | 2 | 1 |
|
SLC37A4 Deletion/Duplication Analysis Baylor Genetics United States | 2 | 1 |
|
Baylor Genetics United States | 2 | 1 |
|
SLC37A4 Sequence Analysis (Prenatal Diagnosis) Baylor Genetics United States | 2 | 1 |
|
Baylor Genetics United States | 842 | 637 |
|
Glycogen Storage Disease Type Ib via the SLC37A4 (G6PT1) Gene PreventionGenetics United States | 2 | 1 |
|
Inherited Metabolic Disorders Panel Dhiti Omics Technologies Private Ltd India | 376 | 317 |
|
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.