# Curate Variants

The **Curate Variants** page is where you review and manage variants added to Curate.

Use **Curate Variants** to:

* Add or delete curated variant annotations
* Review curated variants

![](/files/7zuT87IILb30TPhgidei)

The Curate Variants page consists of:

1. [Curate Navigation panel](/emedgene/emedgene-curate-manual/curate_overview/curate_navigation_panel.md) (left),
2. [Curate Variant table](/emedgene/emedgene-curate-manual/curate_variants/curate_variant_table.md)—lists your curated variants (center),
3. [Curate Variant page](/emedgene/emedgene-curate-manual/curate_variants/curate_variant_page.md)—highlights the most clinically relevant variant information (right).

## Variants supported in Curate

You can add the following variant types to Curate:

* Single nucleotide variants (SNVs)

{% hint style="info" %}
**Note:** For SNVs, the **Uncertain** and **Protein extension** variant effects are not supported.
{% endhint %}

* Small insertions or deletions (indels)
* Copy number variants (CNVs) — deletions and duplications only
* Multi-nucleotide variants (MNVs) in which the reference and alternate alleles differ in length are supported (for example, AA <i class="fa-arrow-right">:arrow-right:</i> TTTT)

The following variant types are not supported:

* Copy number variant insertions (INS)
* Multi-nucleotide variants (MNVs) in which the reference and alternate alleles are the same length are not supported (for example, TTT <i class="fa-arrow-right">:arrow-right:</i> AAA)
* Intergenic variants
* Short tandem repeats (STRs)

## Learn more

<table data-view="cards"><thead><tr><th></th><th></th><th></th></tr></thead><tbody><tr><td><strong>Curate Variant table</strong></td><td>Search, sort, and review variants stored in your organization’s Curate database.</td><td><i class="fa-arrow-up-right-from-square">:arrow-up-right-from-square:</i> <a href="/pages/8hG8ce01J54khFJiCDvf">Learn more</a></td></tr><tr><td><strong>Curate Variant page</strong></td><td>Review interpretation details, pathogenicity, related cases, and network data for a variant.</td><td><i class="fa-arrow-up-right-from-square">:arrow-up-right-from-square:</i> <a href="/pages/zPNkYLeI20AsvBlu5oOX">Learn more</a></td></tr><tr><td><strong>Adding variants to Curate</strong></td><td>Add one variant, upload many variants, or export a variant from Analyze.</td><td><i class="fa-arrow-up-right-from-square">:arrow-up-right-from-square:</i> <a href="/pages/hIKA4tT7VBXt1OoW0efA">Learn more</a></td></tr><tr><td><strong>Curate Variant annotations in the case</strong></td><td>See how Curate data appears in Analyze during case and variant review.</td><td><i class="fa-arrow-up-right-from-square">:arrow-up-right-from-square:</i> <a href="/pages/6zOsdD5DenVyZUTLrKqH">Learn more</a></td></tr><tr><td><strong>Deleting a variant in Curate (v100.39.0+)</strong></td><td>Permanently remove a variant from your organization’s Curate database.</td><td><i class="fa-arrow-up-right-from-square">:arrow-up-right-from-square:</i> <a href="/pages/UBkpWj3m8O3RMEsflIQP">Learn more</a></td></tr></tbody></table>


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