# Variant visualization tool

The variant visualization tool in Emedgene provides a high-resolution, interactive genomic context for variant interpretation. It supports multiple variant types—SNVs, Indels, CNVs, STRs, MRJD, and Targeted Caller Variants—while integrating population data, functional predictions, curated annotations, and sequencing evidence.

An [IGV](http://software.broadinstitute.org/software/igv/home)-based customizable viewer enables visual review of alignment and annotation data for validation and interpretation of variant calls.

The viewer is embedded in the [Visualization tab](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/visualization_section) of the Variant page and is accessible from [Analysis tools tab](https://github.com/illumina-swi/emedgene-docs/blob/prod/docs/emedgene-analyze-manual/reviewing_a_case/analysis-tools-tab/analysis-tools-tab-beta-v100.39.0+) in New mode (v100.39.0+).