> 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/network-summary-card.md).

# Network summary card

## Card contents

The **Network summary card** on the [**Curate Variant page**](/emedgene/emedgene-curate-manual/curate_variants/curate_variant_page.md) shows related variant curations shared by collaborator organizations in your [**Network**](/emedgene/emedgene-analyze-manual/settings/network.md).

For small variants, the card shows occurrences of the same variant. For copy number variants, the card shows overlapping variants.

A variant may be displayed in **Curate variant table** based on network data before it has been added to your own **Curate** database (network-only variant). For network-only variants, the **Network summary card** is the only card shown on the variant page. Use [**Import**](#how-to-import-a-network-only-variant) to add the variant to your **Curate** database.

### Small variants

<figure><img src="https://1131024994-files.gitbook.io/~/files/v0/b/gitbook-x-prod.appspot.com/o/spaces%2FGCW0DnLlE7QjoZPNmKIi%2Fuploads%2Fgit-blob-dd5b045819c950abd8720cdbd621feda140335a6%2Fnetwork%20small.png?alt=media" alt=""><figcaption><p><strong>Network summary card</strong> for a small variant.</p></figcaption></figure>

For small variants, the **Network summary card** features:

* Collaborator (organization name)
* Variant pathogenicity
* Case creation date
* Transcript
* Gene-related disease
* Variant interpretation, shown when you expand a row
* [Import](#how-to-import-a-network-only-variant) option (for network-only variants)

### CNVs

![Network summary 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-2db0b7020b34a6c88c64d37f7e6e814a58782c56%2Fnew%20network%20summary.png?alt=media)

For copy number variants, the table shows all overlapping variants. By default, the annotation overlap range is set to 70–100%, and you can adjust it with the filter.

For copy number variants, the **Network summary card** features:

* Collaborator (organization name)
* Variant details: genomic coordinates and size
* Annotation overlap percentage
* Variant pathogenicity
* Case creation date
* Gene-related disease
* Variant interpretation, shown when you expand a row
* [Import](#how-to-import-a-network-only-variant) option (for network-only variants)

## How to import a network-only variant

You can add a network-only variant to your **Curate** database. If the variant already exists in your **Curate** database, import is not available.

{% hint style="info" %}
You cannot import a variant if it does not have pathogenicity.
{% endhint %}

To add a network-only variant to your **Curate** database, select **Import** in the corresponding row.

**Result:**

* The variant is added to your **Curate** database.
* The import activity is logged in the [**Activities panel**](/emedgene/emedgene-curate-manual/curate_variants/curate_variant_page/activities-panel.md).

After import, you can review and update the local curation as needed.


---

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