> For the complete documentation index, see [llms.txt](https://vci-gci-docs.clinicalgenome.org/vci-gci-docs/llms.txt). Markdown versions of documentation pages are available by appending `.md` to page URLs; this page is available as [Markdown](https://vci-gci-docs.clinicalgenome.org/vci-gci-docs/vci-help/variant-prioritization/data-output.md).

# Data Output

Once variants of interest have been identified, a user can select them using the checkbox on the left side of the main table.

![](https://453646021-files.gitbook.io/~/files/v0/b/gitbook-x-prod.appspot.com/o/spaces%2FzjRMfxI6chghHwy4VhQv%2Fuploads%2Fa10FDW0MF2U3AQDgciBm%2FScreen%20Shot%202022-06-13%20at%202.54.22%20PM.png?alt=media\&token=6ad37a69-2d44-42b1-b113-4ef96106034f)

Users can then use the orange 'Transfer' button to download the selected variants and associated data into a .csv output. 

{% hint style="info" %}
We anticipate having VCI transfer soon. For now users can enter the variant CAID if they wish to continue with curation in the VCI. 
{% endhint %}


---

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