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

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 and analyze your SV with known insertions, deletions, and duplications. Includes tutorials.

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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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