Change log workbench 30

Features:

• Feature | ACMG SNV | Add note

• Feature | Add report service activity in dashboard

• Feature | Add template name change activity in dashboard

• Feature | Add template upload activity in dashboard

• Feature | Import Gene Interpretation from Curate

• Feature | Enable kit management in organization settings

• Feature | New Phenomeld filter added

• Feature | Presets | Gene list | Search for gene list name

• Feature | Var page | Add Genomenon linkout to clinical significance

• Feature | Display varcaller in varpage

• Feature | Varpage | Enrich related cases

• Feature | Gene list | add NCBI ID to genes in gene list in database

• Feature | Validation of variant retrieval. When system is degraded this will alert users not to work on cases with incomplete variant data.

Enhancement:

• Enhancement | Visualization - add tracks order

• Enhancement | Visualization | Change default locus zoom for BigWig

• Enhancement | Add more ethnicities

Bug fixes:

• Bug Fix | Display chr number for finalized cases in finalize tab

• Bug Fix | Add new case | Reactivate batch mode using HPO IDs