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New filters have been added to narrow your search: Test target, to filter by number of genes; Genes and Conditions, to search by gene symbol or condition name; and Labs, to search by a laboratory name.
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Labs matching your search
26 labs with tests matching your search, 1 lab matching in other ways
Results:
81 genetic tests from 26 labs with tests matching your search, 1 lab matching in other ways
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods | |
|---|---|---|---|---|
TNFRSF11A Gene Osteolysis, familial expansile NGS Genetic DNA Test | 1 | 1 |
| |
TNFRSF11A Gene Osteopetrosis, autosomal recessive type 7 NGS Genetic DNA Test | 1 | 1 |
| |
| 1 | 1 |
| ||
| 1 | 1 |
| ||
| 1 | 1 |
| ||
| 1 | 1 |
| ||
| 3 | 1 |
| ||
| 1 | 1 |
| ||
| 1 | 1 |
| ||
| 1 | 1 |
| ||
| 1 | 1 |
| ||
| 2 | 405 |
| ||
| 374 | 386 |
| ||
Multigene panel for skeletal dysplasia based on whole-exome sequencing | 1 | 474 |
| |
Multigene panel for primary immunodeficiencies based on whole-exome sequencing | 1 | 535 |
| |
| 754 | 562 |
| ||
| 624 | 349 |
| ||
| 110 | 50 |
| ||
| 3 | 1969 |
| ||
| 14 | 14 |
|
81 tests from 26 labs
Page 1 of 5❯Osteolysis, familial expansile, 174810, Autosomal dominant; FEO (Familial expansile osteolysis) (TNFRSF11A gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Osteopetrosis, autosomal recessive 7, 612301; OPTB7 (Osteopetrosis-hypogammaglobulinemia syndrome) (TNFRSF11A gene) (Sequence Analysis-All Coding Exons) (Prenatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Paget disease of bone 2, early-onset, 602080, Autosomal dominant; PDB2 (Familial expansile osteolysis) (TNFRSF11A gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Osteopetrosis, autosomal recessive 7, 612301; OPTB7 (Osteopetrosis-hypogammaglobulinemia syndrome) (TNFRSF11A gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
TNFRSF11A Single Gene by Fulgent Genetics
3 conditions, 1 gene
3 conditions, 1 gene
Sanger sequencing of TNFRSF11A by Laboratorio de Genetica Clinica SL
1 condition, 1 gene
1 condition, 1 gene
Sanger sequencing of TNFRSF11A by Laboratorio de Genetica Clinica SL
1 condition, 1 gene
1 condition, 1 gene
Sanger sequencing of TNFRSF11A by Laboratorio de Genetica Clinica SL
1 condition, 1 gene
1 condition, 1 gene
FoundationOne® Heme by Foundation Medicine, Inc.
2 conditions, 405 genes
2 conditions, 405 genes
Inborn Errors of Immunity GenePanel by Mayo Clinic Laboratories, Mayo Clinic
374 conditions, 386 genes
374 conditions, 386 genes
Multigene panel for skeletal dysplasia based on whole-exome sequencing by CGPP - Center for Predictive and Preventive Genetics, IBMC - Institute for Cell and Molecular Biology
1 condition, 474 genes
1 condition, 474 genes
Multigene panel for primary immunodeficiencies based on whole-exome sequencing by CGPP - Center for Predictive and Preventive Genetics, IBMC - Institute for Cell and Molecular Biology
1 condition, 535 genes
1 condition, 535 genes
Invitae Inborn Errors of Immunity and Cytopenias Panel by Labcorp Genetics (formerly Invitae), LabCorp
754 conditions, 562 genes
754 conditions, 562 genes
Invitae Skeletal Disorders Panel by Labcorp Genetics (formerly Invitae), LabCorp
624 conditions, 349 genes
624 conditions, 349 genes
LowBoneDensityZoom by Johns Hopkins Genomics DNA Diagnostic Laboratory, Johns Hopkins University, School of Medicine
110 conditions, 50 genes
110 conditions, 50 genes
qGenEx Intellectual disability by Quantitative Genomic Medicine Laboratories, SL
3 conditions, 1969 genes
3 conditions, 1969 genes
Osteopetrosis NGS panel by HNL Genomics Connective Tissue Gene Tests
14 conditions, 14 genes
14 conditions, 14 genes
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.