These tracks add curated clinical context to the genomic view.
The ClinVar track shows short variants submitted to ClinVar.
The ClinVarSV track shows structural variants submitted to ClinVar.
The Curate track shows short variants that have an entry in the Curate database.
Select a variant to open a popup with:
Clickable variant ID that opens the variant’s Curate page in a new tab
Variant type
Main effect
Chromosome and position or range
Transcript, if available
Gene-related disease
Pathogenicity
The CurateSV track shows structural variants that have an entry in the Curate database.
Last updated 14 days ago
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