ClinVar
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Explore more → **ClinVar**
What is ClinVar?
ClinVar is a freely accessible, public archive of reports of the relationships among human variations and phenotypes, with supporting evidence. It facilitates access to and communication about the relationships asserted between human variation and phenotypes, supporting interpretation of variants found during clinical sequencing.
What other technologies are related to ClinVar?
ClinVar Complementary Technologies
gnomAD
gnomAD provides allele frequencies observed in large population cohorts. This information helps assess the pathogenicity of variants found in ClinVar, making it a complementary resource.
HGMD
No summary available
HGMD (Human Gene Mutation Database) catalogs known germline mutations associated with human inherited disease. It complements ClinVar by providing expert-curated disease-causing mutations, although it has a different scope and curation process.
OMIM
No summary available
OMIM (Online Mendelian Inheritance in Man) is a comprehensive compendium of human genes and genetic phenotypes. It is complementary to ClinVar because it provides detailed information about diseases and their genetic basis, which can help interpret variants in ClinVar.
Number of organizations that mention technology
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Which job functions commonly mention ClinVar?
Bioinformatics
0.7% of all Bioinformatics jobs mention ClinVar
View 84
jobs on Sumble
Bioinformatician
0.3% of all Bioinformatician jobs mention ClinVar
View 11
jobs on Sumble
Geneticist
0.3% of all Geneticist jobs mention ClinVar
View 2
jobs on Sumble
Biologist
0.2% of all Biologist jobs mention ClinVar
View 91
jobs on Sumble
Scientist
129 Scientist jobs mention ClinVar
View 129
jobs on Sumble
Which organizations are mentioning ClinVar?
NYU Langone Health
Health Care and Social Assistance
University of North Carolina at Chapel Hill
Educational Services
Frederick National Laboratory for Cancer Research
Public Administration
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