Requested annotations for non-redundant variant data

[thefferon]

The following annotations would be really useful for the non-redundant variants:

• overlap with genes
• repeat regions and segmental duplication regions
• overlap with known dosage sensitive genes
• overlap with known clinical variants, e.g., from ClinVar

I'm sure there are a lot more.

[JohnG-001]

overlap with genes

NR SV data Files are now available showing overlap with ACMG genes. E.g.:
GRCh38.nr_deletions.acmg_genes.tsv.gz

overlap with known clinical variants, e.g., from ClinVar

NR SV files now include: clinical_assertion and clinvar_accession fields.

More work in all of the areas mentioned is under consideration.