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dbVar is NCBI's database of genomic structural variation – insertions, deletions, duplications, inversions, mobile element insertions, translocations, and complex chromosomal rearrangements

NEW! Human Structural Variation Data Hub

For easy access to dbVar's most frequently accessed data, visit our new Human 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, take a moment to send us your ideas on making this new page even 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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