---
title: How do I sort variants in the variants table?
description: Learn about the available sorting options and how to apply them to prioritize your variant review.
---
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# How do I sort variants in the variants table?
## Learn about the available sorting options and how to apply them to prioritize your variant review.
Sorting options are accessible from the drop-down menu in the top right-hand corner of the variants table. For each option, you can switch between ascending and descending order using the sort icon. By default, all options sort in descending order, except **Locus**, which sorts in ascending order.
The available sorting options are:
**DiagAI Score** — Applied by default in germline analyses (for analyses run after October 2, 2024). Sorts variants by their DiagAI prioritization score.
**SeqOne Rank+** — The previous AI-based prioritization algorithm, applied by default to analyses run before October 2, 2024. Still available for those analyses.
**VariAction Rank** — Available in SomaVar analyses (v1.8+). Prioritizes somatic variants based on clinical actionability using JaxCKB annotations, taking into account the variant's impact, ComPerMed score, AMP tier, and match with the patient's indication.
**ACMG** — Sorts variants from Pathogenic (class 5) to Benign (class 1).
**Locus** — Sorts variants by genomic position, in ascending order by default.
**Gene** — Sorts variants alphabetically by gene name. For multi-gene variants, the gene with the highest impact is used.
**Allele Frequency** — Sorts by VAF in descending order by default.
**GnomAD Allele Frequency / Allele Count** — Sorts by GnomAD AF or AC in ascending or descending order.
💡 To manually check for compound heterozygous variants, sort by **Gene** or **Locus** to group same-gene variants together.
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