> 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-analyze-manual/variant-visualization/variant-visualization-tool/visualization-tracks/curated-data-tracks.md).

# Curated data tracks

These tracks add curated clinical context to the genomic view.

## ClinVar

The **ClinVar** track shows short variants submitted to ClinVar.

<figure><img src="/files/aQiCAeBIOgRnvDsoMOZZ" alt=""><figcaption><p><strong>ClinVar</strong> track</p></figcaption></figure>

## ClinVarSV

The **ClinVarSV** track shows structural variants submitted to ClinVar.

<figure><img src="/files/gJJQTXI3Noia29cUGfIx" alt=""><figcaption><p><strong>ClinVarSV</strong> track</p></figcaption></figure>

## Curate

The **Curate** track shows short variants that have an entry in the [Curate database](/emedgene/emedgene-curate-manual/curate_variants.md).

Select a variant to open a popup with:

* Clickable variant ID that opens the variant’s Curate page in a new tab
* Variant type
* Main effect
* Chromosome and position or range
* Transcript, if available
* Gene-related disease
* Pathogenicity

<figure><img src="/files/uifGHHL5pTcJBeb2R0Eo" alt=""><figcaption><p><strong>Curate</strong> track</p></figcaption></figure>

## CurateSV

The **CurateSV** track shows structural variants that have an entry in the [Curate database](/emedgene/emedgene-curate-manual/curate_variants.md).

<figure><img src="/files/SZ5wDGhO9ho6bJ4p05Lz" alt=""><figcaption><p><strong>CurateSV</strong> track</p></figcaption></figure>


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