dbVar

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

Getting Started

Accessing Data

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New Data!

dbVar recently added six new studies and updated the Clinical Structural Variants study (nstd102). Please go to the Study Browser or our Structural Variation Data Hub to start exploring. As always, all dbVar data are available via FTP. Please email us if you have any questions.

Search Examples (additional terms)

Gene	PTEN[Gene Name]
Genomic location	6[Chr] AND (1500000:3000000[ChrPos] OR 1500000:3000000[ChrEnd])
Gene in a specific dataset	CFTR[Gene Name] AND "1000 Genomes"[Study]
Clinical significance and phenotype	((Pathogenic[Clinical Interpretation]) OR "Likely pathogenic"[Clinical Interpretation]) AND autism[Clinical Phenotype]
All of dbVar (then use filters on results page)	all[sb]