> For the complete documentation index, see [llms.txt](https://help.bioinsight.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.bioinsight.illumina.com/connected-insights/interpret-and-report/add-variant.md).

# Add Variant

If you ever notice an inaccurate variant call or have additional variants from another test to report, small variants and copy number variants can be added to the case at any time, ensuring your analyses are both accurate and comprehensive.

1. Navigate to the [Case Page](/connected-insights/interpret-and-report/inter-introduction.md) of a case.
2. Towards the upper right corner of the interface, click the "+" icon.![](https://1917818526-files.gitbook.io/~/files/v0/b/gitbook-x-prod.appspot.com/o/spaces%2FrkSuX7Vmcc4W5JjlZQyx%2Fuploads%2Fgit-blob-68630f7f20ac84f7a0e2e6fcf419c78f398a1856%2Fimage%20\(20\).png?alt=media)
3. Click **Add Variant**.
4. Read the instructions and complete the form. Required fields are indicated with an asterisk (\*).

Note that a variant can be added from any tab within the case, such as on the [Visualize Tab](/connected-insights/interpret-and-report/cm-visualize-tab.md). The "+" icon is also accessible when a [Biomarker Details](/connected-insights/interpret-and-report/viewdetails-introduction.md) page overlay is open; simply pull down the overlay to reveal.

A Karyotype can also be added from the "+" icon. See [Results / Overview Tab](/connected-insights/interpret-and-report/cm-overview-tab.md) for additional info on Karyotype.


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