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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

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Submitting Data

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]

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