> For the complete documentation index, see [llms.txt](https://help.connected.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.connected.illumina.com/emedgene/emedgene-curate-manual/curate_variants/curate_variant_page/related-cases-card.md).

# Related cases card

## Card contents

The **Related cases card** of the [**Curate Variant page**](/emedgene/emedgene-curate-manual/curate_variants/curate_variant_page.md) shows cases in your organization that include the same small variant or overlapping copy number variants.

### Small variants

<figure><img src="https://1131024994-files.gitbook.io/~/files/v0/b/gitbook-x-prod.appspot.com/o/spaces%2FGCW0DnLlE7QjoZPNmKIi%2Fuploads%2Fgit-blob-0bbdc597d550be77f15e277d1d9f768450b29316%2FRelated%20small.png?alt=media" alt=""><figcaption><p><strong>Related cases card</strong> for a small variant.</p></figcaption></figure>

For small variants, the **Related cases card** includes:

* Case ID and genome reference
* Variant pathogenicity
* Case creation date
* Variant tag
* Variant inheritance
* Analysis type
* Case link

### CNVs

![Related cases card for a copy number variant.](https://1131024994-files.gitbook.io/~/files/v0/b/gitbook-x-prod.appspot.com/o/spaces%2FGCW0DnLlE7QjoZPNmKIi%2Fuploads%2Fgit-blob-bcf40a3ebddc86c40fcc3f33545ef842d317f396%2Frelated%20cases.png?alt=media)

For copy number variants, the table shows all overlapping variants.

By default, the CNV overlap ranges are set to 70–100%, and you can adjust them with the filter.

For copy number variants, the **Related cases card** shows the same case and variant details as for small variants, plus the following fields:

* Overlapping variants' genomic coordinates and size
* CNV overlap percentages


---

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