> 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_table.md). # Curate Variant table The **Curate Variant table** displays all variants stored in your organization’s **Curate** database. Use it to review variants at a glance. You can: * Sort the table by any column * Reorder columns by drag-and-drop * Adjust column width

## Search box Use the search box above the **Curate Variant table** to quickly find variants. You can search by: * **Gene symbol** (e.g., `BRCA1`) * **Genomic position** (e.g., `chr17:43071077`) * **Variant type** (e.g., `SNV`, `DEL`, `DUP`) The table updates automatically based on your search. {% hint style="info" %} **Note:** CNV variants are included in results when the searched gene or position falls within the CNV range. {% endhint %} ## Variant table columns The **Curate Variant table** displays all variants stored in your organization's **Curate** database, along with key variant identifiers, pathogenicity classifications, and network interpretation data.


Gene	Gene identifier. SNV/Indel/single-gene CNV: An HGNC-approved gene symbol Multi-gene CNVs: A list of HGNC-approved gene symbols and the number of genes included if only part of the list is shown. Tip: If only the beginning of the list is displayed in the table, you can see the full gene list in the pop-up tooltip. Supports alphabetical sorting.
Type	Specifies whether the variant is SNV, Indel, CNV, SV, STR, or other. Supports alphabetical sorting.
Variant Details	Displays genomic coordinates and basic variant identifiers. Variant details reflect the genome reference selected in the left navigation panel. SNV/Indel: Genomic position, nucleotide change, and dbSNP ID CNV/SV: Genomic coordinates and variant size Supports sorting by genomic start location.
Pathogenicity	Pathogenicity classification. Supports alphabetical sorting.
Network	Displays pathogenicity classifications assigned by partnering organizations. The column uses a color-coded indicator that summarizes how the variant is classified across the network: Red: Pathogenic or Likely Pathogenic. Orange: VUS. Green: Benign or Likely Benign. Mixed colors: Connected organizations have assigned conflicting classifications. No indicator: No connected organization has assigned classification. Tip: hover over the badge to see pathogenicity. Supports alphabetical sorting.

[^1]: HUGO Gene Nomenclature Committee --- # Agent Instructions This documentation is published with GitBook. GitBook is the documentation platform designed so that both humans and AI agents can read, navigate, and reason over technical content effectively. Learn more at gitbook.com. ## Querying This Documentation If you need additional information that is not directly available in this page, you can query the documentation dynamically by asking a question. Perform an HTTP GET request on the current page URL with the `ask` query parameter, and the optional `goal` query parameter: ``` GET https://help.connected.illumina.com/emedgene/emedgene-curate-manual/curate_variants/curate_variant_table.md?ask=&goal= ``` `ask` is the immediate question: it should be specific, self-contained, and written in natural language. `goal` is optional and describes the broader end goal you are ultimately trying to accomplish on behalf of the user. GitBook uses it to tailor the answer towards what is most useful for that goal. The response will contain a direct answer to the question and relevant excerpts and sources from the documentation. Use this mechanism when the answer is not explicitly present in the current page, you need clarification or additional context, or you want to retrieve related documentation sections.