> 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/emedgene/emedgene-curate-manual/curate_variants/curate_variant_table.md). # Curate Variant table The **Curate Variant table** lists variants in your organization’s **Curate** database and variants shared by collaborators. * **Local variants** are stored in your organization’s **Curate** database. * If collaborators have shared curations for your local variant, they will appear in the **Network summary card.** You cannot import these curations for an existing variant but you can copy shared information. * **Network-only variants** are shared by collaborators but are not stored in your organization’s **Curate** database. * The **Variant page** for a network-only variant includes only the **Network summary card** and limited shared annotations. Select **Import** to add the variant to your database. Before import, its annotations do not appear in **Analyze**. 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. The table updates automatically based on your search. You can search by: * **Gene symbol** (e.g., `BRCA1`).\ A gene symbol search returns SNVs and any CNVs whose range include that gene. * **Genomic position** (e.g., `chr17:43071077`).\ A genomic position search returns SNVs and any CNVs whose range include that position. * **Variant type** (e.g., `SNV`, `DEL`, `DUP`) * **Coding DNA change** (v100.41+) (e.g., partial `c.5266` or full change `c.5266C>T`; you do not enter a transcript).\ A coding DNA change search can return more than one result when the same value is found on more than one transcript. * **Protein change** (v100.41+) (e.g., partial `p.Arg1751` or full change `p.Arg1751Ter`; you do not enter a transcript).\ A protein change search can return more than one result when the same value is found on more than one protein reference.

A coding DNA change search can return more than one result when the same value is found on more than one transcript.

## Variant table columns The **Curate Variant table** displays local and network-only variants, along with key variant identifiers, curation status (v100.41+), pathogenicity classification, and network interpretation data. Select a row to open the **Curate Variant page**.


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.
Status (v100.41+)	Curation status of the variant. For network-only variants, the column shows NA. Supports alphabetical sorting, with NA first.
Pathogenicity	Pathogenicity classification. Supports alphabetical sorting.
c. (v100.41+)	Coding DNA change for the variant’s selected transcript. SNV/indel variants only.
p. (v100.41+)	Protein change for the variant’s selected transcript. SNV/indel variants only.
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.

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