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dbVar is NCBI's database of human genomic Structural Variation — large variants >50 bp including insertions, deletions, duplications, inversions, mobile elements, translocations, and complex variants

Announcing the dbVar Public Track Hub! dbVar has released a track hub containing curated datasets of Clinical SV and Common SV. You can view data summaries at the preceding links, and browse the new tracks using NCBI's Variation Viewer or by connecting to the Public dbVar Hub at the UCSC Genome Browser.

Our Clinical SV Walkthrough Page shows you how to visualize and explore known clinical structural variants, and more generally how to navigate our resource.

dbVar's Non-redundant (NR) SV files on GitHub allow you to compare your SV with known insertions, deletions, and duplications. Includes tutorials.

Search Examples (additional terms)

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dbVar Webinar (Part 1 of 2)

dbVar Webinar (Part 2 of 2)

dbVar Data in Variation Viewer

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