> For the complete documentation index, see [llms.txt](https://help.bioinsight.illumina.com/llms.txt). Markdown versions of documentation pages are available by appending `.md` to page URLs; this page is available as [Markdown](https://help.bioinsight.illumina.com/emedgene/emedgene-analyze-manual/variant_page/related_cases_section.md).

# Related cases tab

The **Related Cases tab** highlights [tagged](/emedgene/emedgene-analyze-manual/variant_page/variant_tagging_widget.md) variants found in previously analyzed cases, both within your organization and among organizations in your [network(s)](/emedgene/emedgene-analyze-manual/analyze_network.md).

{% hint style="info" %}
**Note:** data is automatically lifted over between genome references on the fly.
{% endhint %}

## Key features:

* [Network data view controls](/emedgene/emedgene-analyze-manual/variant_page/related_cases_section/network-data-view-controls.md): Enable viewing of network-wide case data alongside internal case data.
* [Pathogenicity trend bar](/emedgene/emedgene-analyze-manual/variant_page/related_cases_section/pathogenicity-trend-bar.md): Visualizes the distribution of classification outcomes for a variant across previously analyzed cases.
* [CNV overlap percentage filter](/emedgene/emedgene-analyze-manual/variant_page/related_cases_section/cnv_overlap_percentage.md): Allows to dynamically filter CNVs by overlap percentage.
* [Related cases table](/emedgene/emedgene-analyze-manual/variant_page/related_cases_section/related-cases-table.md): Summarizes key details of previous variant interpretations.

{% hint style="info" %}
**Related Cases tab** is not available for haplotype, TRA (v100.41+) and INV (v100.41+) variant types and for BND (v100.41+) records.
{% endhint %}


---

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