Filter by Variant Category

Connected Insights provides users with the flexibility to apply a selection of filter criteria to each variant category supported in the software. The selection of variant categories impacts the set of filtering criteria that can be selected for a given filter group.

The following table summarizes filters available for each variant category:

Variant Categories

Variant Category	Small Variants	Structural Variants	Copy Number Variants	RNA Splice Variants	RNA Fusion Variants
COSMIC	+
CGC	+	+	+	+	+
Cancer Hotspots	+	+	+	+	+
Change (Copy Number)			+
Change (Fold Change)			+
ClinVar (VCV, RCV)	+	+	+	+	+
Consequences	+	+	+	+	+
Constraint Metrics(gnomAD)	+	+	+	+	+
Filters	+	+	+	+	+
Flags	+	+	+	+	+
Genes	+	+	+	+	+
Haploinsufficiency(ClinGen)	+	+	+	+	+
Length	+	+	+	+	+
Low Complexity Region(gnomAD)	+
OMIM	+	+	+	+	+
Origin	+	+	+	+	+
Population	+	+	+
Position (Chromosome)	+	+	+	+	+
Position (Genomic Regions)	+	+	+	+	+
PrimateAI-3D	+
LOH Overlap	+	+	+	+	+
Sample Metrics	+	+	+	+	+
Splice AI	+
Triplosensitivity (ClinGen)	+	+	+	+	+
Variant Type	+	+	+