ClinVar Variants Track Settings
ClinVar Variants   (All Phenotype and Literature tracks)

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ClinVar is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the ClinVar database is open to all academic users, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions.

This track shows the genomic positions of variants in the ClinVar database. ClinVar is a free, public archive of reports of the relationships among human variations and phenotypes, with supporting evidence.

Display Conventions and Configuration

Genomic locations of ClinVar variants are labeled with the ClinVar name. All information related to each is variant is shown on that variant's details page.


ClinVar files were reformatted at UCSC to the bigBed format.


Thanks to NCBI for making the ClinVar data available on their FTP site.