# Reviewing a variant - [Variant page](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/variant_page.md) - [Variant page top bar](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/variant_page_top_bar.md) - [Variant tagging widget](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/variant_page_top_bar/variant_tagging_widget.md) - [Multiple tags](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/variant_page_top_bar/variant_tagging_widget/multiple-tags.md) - [Curate actions in Analyze](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/variant_page_top_bar/curate-actions-in-analyze.md) - [Export to Curate](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/variant_page_top_bar/curate-actions-in-analyze/export-to-curate.md) - [Update in Curate (v38.0+)](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/variant_page_top_bar/curate-actions-in-analyze/update-in-curate-v38.0+.md) - [Open in Curate](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/variant_page_top_bar/curate-actions-in-analyze/open-in-curate.md) - [Summary tab](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/summary_section.md) - [Clinical significance tab](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/clinical_significance_section.md) - [Variant info](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/clinical_significance_section/variant-info.md) - [Transcript](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/clinical_significance_section/variant-info/transcript.md) - [Resources](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/clinical_significance_section/variant-info/resources.md) - [In silico predictions](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/clinical_significance_section/in-silico-predictions.md) - [Gene metrics](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/clinical_significance_section/gene-metrics.md) - [Clinical significance](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/clinical_significance_section/clinical-significance.md) - [Gene-related diseases](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/clinical_significance_section/gene-related-diseases.md) - [Quality tab](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/quality_section.md) - [Variant quality summary](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/quality_section/variant-quality-summary.md): Understand the overall quality signal shown for a variant across samples. - [Quality metrics per variant type](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/quality_section/quality-metrics-per-variant-type.md) - [SNV, MNV, and indel quality metrics](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/quality_section/quality-metrics-per-variant-type/snv-mnv-and-indel-quality-metrics.md) - [CNV quality metrics](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/quality_section/quality-metrics-per-variant-type/cnv-quality-metrics.md) - [SV quality metrics](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/quality_section/quality-metrics-per-variant-type/sv-quality-metrics.md) - [STR quality metrics](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/quality_section/quality-metrics-per-variant-type/str-quality-metrics.md) - [Haplotype variant quality metrics](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/quality_section/quality-metrics-per-variant-type/haplotype-variant-quality-metrics.md) - [Allele distribution](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/quality_section/allele-distribution.md): Review how sequencing reads support reference and alternate alleles. - [Visualization tab](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/visualization_section.md) - [Population statistics tab](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/population_statistics_section.md) - [Connected variants tab](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/connected-variants-tab.md) - [Related cases tab](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/related_cases_section.md) - [Network data view controls](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/related_cases_section/network-data-view-controls.md) - [Pathogenicity trend bar](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/related_cases_section/pathogenicity-trend-bar.md) - [Related cases table](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/related_cases_section/related-cases-table.md) - [CNV overlap percentage filter](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/related_cases_section/cnv_overlap_percentage.md) - [One-way CNV annotation overlap](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/related_cases_section/cnv_overlap_percentage/one-way-cnv-annotation-overlap.md) - [Evidence tab](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/evidence_section.md) - [ACMG SNV Classification wizard](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/evidence_section/acmg_snv_classification_wizard.md) - [Logic behind ACMG classification of SNVs](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/evidence_section/logic_behind_acmg_classification_of_snvs.md) - [Individual ACMG criteria evaluation](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/evidence_section/individual-acmg-criteria-evaluation.md) - [ACMG CNV Classification wizard](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/evidence_section/acmg_cnv_classification_wizard.md) - [Variant page sidebar](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/variant_page_sidebar_-229+.md) --- # Agent Instructions: 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: ``` GET https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page.md?ask= ``` The question should be specific, self-contained, and written in natural language. 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.