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 is a free, public archive of reports
of the relationships among human variations and phenotypes, with supporting
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.