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

Return to Default browser tracks.

This tool is for research use only. For personal medical or genetic advising, consult a qualified physician.