dbVar is NCBI's database of human genomic structural variation — insertions, deletions, duplications, inversions, mobile elements, and translocations

Structural Variation Data Hub

For easy access to dbVar's most frequently accessed data, visit our Structural Variation Data Hub, where you will find links to useful Clinical Structural Variation, Population-based surveys of common structural variation, and our Top Ten most frequently accessed datasets. While you're there, please take a moment to send us your ideas on how to make the page more helpful!

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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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