> For the complete documentation index, see [llms.txt](https://docs.omics.ai/products/llms.txt). Markdown versions of documentation pages are available by appending `.md` to page URLs; this page is available as [Markdown](https://docs.omics.ai/products/workbench/variant-interpreter/reviewing-variants.md).

# Reviewing variants

The Variant Interpreter organizes findings by variant class, each on its own tab, because each class is called by a different method and evaluated with different evidence. Use the page that matches what you're reviewing:

* [Small variants (SNVs & indels)](/products/workbench/variant-interpreter/reviewing-variants/small-variants.md)
* [Structural variants](/products/workbench/variant-interpreter/reviewing-variants/structural-variants.md)
* [Copy number](/products/workbench/variant-interpreter/reviewing-variants/copy-number.md)
* [Tandem repeats](/products/workbench/variant-interpreter/reviewing-variants/tandem-repeats.md)
* [Paralogs](/products/workbench/variant-interpreter/reviewing-variants/paralogs.md)

Every tab shares the same pattern: a filtered variant list, with visualizations where the class benefits from them, and a detail view where you explore the affected gene, review its [annotation panels](/products/workbench/variant-interpreter/reviewing-variants/annotation-panels.md), open the [genome browser (IGV)](/products/workbench/variant-interpreter/reviewing-variants/genome-browser.md), and [classify](/products/workbench/variant-interpreter/classifying-variants.md) the variant. Classifying a variant makes it eligible for the [report](/products/workbench/variant-interpreter/generating-a-report.md). The sample drawer is available on every tab for context.

Across every class, the workflow has already applied a population-frequency filter so that common variants are removed before you review. How that filter is set is described in [Filtering & prioritization](/products/workbench/variant-interpreter/filtering-and-prioritization.md).


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