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Bookmark or Share- ClinVar - National Center for Biotechnology InformationIf you have questions about the information contained on this website, please see a health care professional. More information about NCBI's disclaimer policy is available. National Library of Medicine 8600 Rockville Pike Bethesda, MD 20894. ClinVar archives and aggregates information about relationships among variation and human health.
- ClinVar - WikipediaClinVar is a public archive with free access to reports on the relationships between human variations and phenotypes, with supporting evidence. The database includes germline and somatic variants of any size, type or genomic location. Interpretations are submitted by clinical testing laboratories, research laboratories, locus-specific databases ...
- How to search ClinVar - National Center for Biotechnology InformationJust type your search term and click on the Search button to the right of the search box. ClinVar can be searched with terms like: gene symbols, e.g. PTEN. gene symbol and c. or p., e.g., mutyh c.1187g>a. location / chromosome coordinates, e.g., chr1:11,102,837-11,267,747, 2:144,213,941 - 144,690,824, etc.
- ClinVar - ClinGen | Clinical Genome ResourceClinVar is a a freely accessible, public archive of reports of the relationships among human variations and phenotypes hosted by the National Center for Biotechnology Information (NCBI) and funded by intramural National Institutes of Health (NIH) funding.
- FAQ about using ClinVar - National Center for Biotechnology InformationClinVar is an archive for classification made by our submitters. Submitters may disagree on how a variant should be classified; read more about how ClinVar calculates consensus and conflicts in different types of classifications. ClinVar does not arbitrate and resolve these conflicts.
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