Got cart: 245 elements, userId=(null) (=cookie), sessionId=2389900827_TQYMgpJse13kaBd1Y0wSwnGyvQbF: 123 millis Startup (bottleneck delay 0 ms, not applied if under 10000) : 0 millis before chromAliasSetup: 0 millis after chromAliasSetup: 37 millis
Done with trackForm: 3 millis
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These links provide track sets selected and pre-configured for specific user scenarios. They are designed to be useful at different genomic loci. Clicking a link below will create a browser window with these tracks visible, without changing the locus.
Clinical SNVs: Assess potential disease contributions of single nucleotide variants in coding regions
Clinical CNVs: Assess potential disease contributions of structural variants in coding regions
Non-coding SNVs: Investigate functional aspects of non-coding variants
Problematic Regions: Evaluate if annotations are on potential low confidence regions due to high homology or other reported concerns
ENIGMA BRCA1/BRCA2 VCEP: Asses potential disease contribution of variants on BRCA1 and BRCA2 according to the ENIGMA VCEP guidelines