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| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Hereditary Hemolytic Anemia Comprehensive Sequencing, Varies Mayo Clinic Laboratories Mayo Clinic United States | 41 | 40 |
|
BloodGenetics Spain | 33 | 36 |
|
Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins University, School of Medicine United States | 107 | 96 |
|
ANK1 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
|
Bone Marrow Failure / Anemia Panel Centogene AG - the Rare Disease Company Germany | 212 | 212 |
|
Centogene AG - the Rare Disease Company Germany | 829 | 848 |
|
Invitae Red Blood Cell Membrane Disorders and Enzymopathies Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 57 | 28 |
|
Invitae Hereditary Hemolytic Anemia Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 77 | 39 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Hereditary Hemolytic Anemia Panel PreventionGenetics, part of Exact Sciences United States | 44 | 34 |
|
Spherocytosis/Elliptocytosis Panel PreventionGenetics, part of Exact Sciences United States | 8 | 6 |
|
Hereditary Spherocytosis Type 1 via the ANK1 Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
|
Fulgent Genetics United States | 61 | 24 |
|
CeGaT GmbH Germany | 14 | 33 |
|
Hemolytic Anemia Panel by next-generation sequencing (NGS) Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States | 33 | 34 |
|
Hereditary spherocytosis type 1 Bioarray Spain | 1 | 1 |
|
ANK1 Deletion/duplication analysis Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States | 1 | 1 |
|
Fulgent Genetics United States | 1 | 1 |
|
Hereditary Spherocytosis NGS Panel Fulgent Genetics United States | 10 | 5 |
|
Fulgent Genetics United States | 5130 | 4674 |
|
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.