Minor build 38 - related fixes and other improvements and fixes

[4.112]

Added

• Contigs on exported variants VCF files (managed and causative variants) (#6310)
• INFO tags for exported variant category EXPORT_CATEGORY on exported variants VCF files (#6324)
• On variant page, display status and status tags from matching causatives' case (#6315)
• Clearer logs reporting case ID when variant loading fails (#6329)
• Export causatives to managed variants infile via CLI, filtering variants by date (#6290, #6338)
• MitoSAlt/SAltShaker SV caller for MT SV variants (#6333)
• Filter selections remain visible in the UI after panel editing actions (#6305)

Changed

• Display genome build on managed variants page (#6297)
• Improve causatives page performance by removing duplicate case query (#6312)
• Display case tags (provisional, diagnostic, incidental, etc) on causatives and verified variants pages (#6312)
• Matching variants (causatives, managed) on the variant page are folded by default (#6346)

Fixed

• Compress demo case rnafusion VCF and add an index (#6292)
• Adding single managed variants with build 38 (#6300)
• Paraphase region names alphabetically sorted on SMN/Dark regions page (#6301)
• "likely benign" classification overwrites "benign" for ACMG (#6325)
• Show pending comments for gene panels (#6327)
• Warnings due to default build 37 used during variants loading even if case has build 38 (#6322, #6331 and #6348)
• Removed unused imports on commands/export/variant module (#6334)
• Region load command to auto-detect VCF chromosome prefix (#6343)
• Search SNVs & SVs by gene when gene is only present on build 38 (#6340)