dbVar

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

Getting Started

Overview of Structural Variation
Organism List
FAQ
Help
Factsheet

Accessing Data

Human Structural Variation Data Hub
Tools for analyzing dbVar data
Study Browser
Genome Browser
FTP Data Download

Other NCBI Resources

dbSNP
ClinVar
Variation Portal
Variation Tools

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!