| left 10% | ctrl+j | track search | t then s | |
| left 1/2 screen | j | default tracks | d then t | |
| left one screen | J | default order | d then o | |
| right 10% | ctrl+l | hide all | h then a | |
| right 1/2 screen | l | custom tracks | c then t | |
| right one screen | L | track collections | t then c | |
| jump to position box | / | track hubs | t then h | |
| zoom in 1.5x | ctrl+i | configure | c then f | |
| zoom in 3x | i | reverse | r then v | |
| zoom in 10x | I | resize | r then s | |
| zoom in base level | b | refresh | r then f | |
| zoom out 1.5x | ctrl+k | view chrom names | v then s | |
| zoom out 3x | k | send to external tool | s then t | |
| zoom out 10x | K | exon view | e then v | |
| zoom out 100x | 0 | default view | d then v | |
| zoom to ... | view DNA | v then d | ||
| 50bp (1 zero) | 1 | Reset all User Settings | c then r | |
| 500bp (2 zeros) | 2 | Tools - BLAT | t then b | |
| 5000bp (3 zeros) | 3 | Tools - Table Browser | t then t | |
| 50kbp (4 zeros) | 4 | Tools - PCR | t then i | |
| 500kbp (5 zeros) | 5 | My Sessions | s then s | |
| 5Mbp (6 zeros) | 6 | Public Sessions | p then s | |
| highlight all (mark) | h then m | clear all Highlights | h then c | |
| quick connect hub | c then h |
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
- Determine Exon Relevance: Examine if variants are present in an exon required for the function of the expressed gene product
- Problematic Regions: Evaluate if annotations are on potential low confidence regions due to high homology or other reported concerns
- ENIGMA BRCA1/BRCA2 VCEP: Assess potential disease contribution of variants on BRCA1 and BRCA2 according to the ENIGMA VCEP guidelines
- InSiGHT Lynch Syndrome VCEP: Assess potential disease contribution of variants on MLH1, MSH2, MSH6, and PMS2 according to the InSiGHT VCEP guidelines
Return to Default browser tracks.
This tool is for research use only. For personal medical or genetic advising, consult a qualified physician.