# Related cases table

The Related cases table provides quick access to variant and case-specific details of previous variant interpretations, both within your organization and among organizations in your [network(s)](/emedgene/emedgene-analyze-manual/analyze_network.md). The table shows key data at a glance, with more detailed information available when you click on a row.

![](/files/t6d9s93zTGkq6U8sbGzT)

## Related cases table columns

<table><thead><tr><th width="197.54547119140625">Column or element</th><th>Details</th></tr></thead><tbody><tr><td><strong>Collaborator</strong></td><td><p>The organization from which the case originates.</p><p>Either your organization or the collaborating organization that is part of your <a href="/pages/BuHJgO3QryxWJGMgrJi8">network</a></p></td></tr><tr><td><strong>Case status icon</strong></td><td><p><img src="/files/y70NcUrDpNed33aTlf49" alt="" data-size="line"> Resolved—The case is <a href="/pages/Qy9LKMN01NOJVyG1lfE9">finalized</a> and the case interpretation status is Confidently Solved, Likely Solved, or Further Investigation</p><p><img src="/files/GA2EK4FpmQxAN9Q5dik1" alt="" data-size="line"> Not resolved—The case is <a href="/pages/Qy9LKMN01NOJVyG1lfE9">finalized</a> and the case interpretation status is Case is not solved</p><p><img src="/files/FHHZttW9joH5zL8euSUq" alt="" data-size="line"> Not finalized—The case is still in review</p></td></tr><tr><td><strong>Case ID</strong></td><td><p>The <a href="/pages/HepXBSl4bnJcL8RkDtCF">Case ID</a> and the reference genome used.</p><p><img src="/files/wLwNvYIT81KF2JPeMuBN" alt="" data-size="line"> The lock icon is displayed next to the Case ID for cases that have <a href="/pages/w1geKQlPQm9DdV3EXN1Q">opted out</a> of <a href="/pages/p8Kigj3aWOc37jfPiHHG">extended sharing</a></p></td></tr><tr><td><strong>Variant details (CNVs)</strong></td><td>Displays variant coordinates and a corresponding genome reference, along with the CNV length</td></tr><tr><td><strong>Overlap (CNVs)</strong></td><td>CNV <a href="/pages/XcG54wrfRD1jRMDLZDpA">annotation overlap</a> percentage</td></tr><tr><td><strong>Pathogenicity</strong></td><td>Previously assigned <a href="/pages/Ou0qaNedUbHGE144vigi">pathogenicity</a></td></tr><tr><td><strong>Date</strong></td><td>The date the case was created</td></tr><tr><td><strong>Tag</strong></td><td>Previously assigned <a href="/pages/rfCptomeVmzD1Ftt75RH">variant tag</a></td></tr><tr><td><strong>Zygosity</strong></td><td>Variant zygosity in the proband and other case samples. Bold text indicates an affected individual</td></tr><tr><td><strong>Link to case search</strong></td><td>Available for cases from your organization.<br><img src="/files/gXSGBfj1wdwR0zOsEwRb" alt="" data-size="line">Clicking the link icon opens the <a href="/pages/QjWGG0vWFqi7uxFrAvBS">Cases tab</a> in a new browser window, filtered by the respective Case ID. This allows you to quickly access and review full <a href="/pages/6BCnvC2ZyRLkfVuxQnUM">case details</a></td></tr><tr><td><strong>Collaborator's contact</strong></td><td>Want to contact a collaborator from your <a href="/pages/kU12Gc7SpSZ8ZFDKF99D">network</a>?<br><img src="/files/qyucG9dkRYxCVwFgcptB" alt="" data-size="line">Click the letter icon to copy their email address to your clipboard</td></tr></tbody></table>

## Detailed information (row click)

Clicking on a row reveals additional variant and case-specific details, including:

* [Variant Interpretation](/emedgene/emedgene-analyze-manual/variant_page/evidence_section.md)
* [ACMG tags](/emedgene/emedgene-analyze-manual/variant_page/evidence_section.md)
* [Selected disease](/emedgene/emedgene-analyze-manual/reviewing_a_case/evidence_page.md)
* Proband ID
* Proband phenotypes
* Proband age
* Proband sex
* Maternal and paternal ethnicity
* Case type


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