Variant page
Navigate between variants using the left and right arrow keys on your keyboard, or click the arrows on either side of the Variant page.
The Variant page showcasing the comprehensive variant information is accessible from the Variant table by selecting the corresponding variant row with a click.
Navigate between variants using the left and right arrow keys on your keyboard, or click the arrows on either side of the Variant page.
The Variant page is comprised of:
Navigation panel (left).
Page body:
Summary tab. Highlights core variant-related information from other tabs
Clinical Significance tab. Reports essential variant- and gene-level information and indicates gene-related diseases.
Quality tab. Outlines the major variant quality parameters in each sample and demonstrates the family tree with the zygosity for each sequenced sample.
Visualization tab. Features the IGV-based BAM file viewer.
Population Statistics tab. Addresses alternative allele frequency, alternative allele count, and the number of homozygotes in public and internal databases.
Connected variants tab. Highlights connections between the examined variant and other variants in the case.
Related Cases tab. Displays statistics regarding the pathogenicity and tags assigned to the variant under review, incorporating data from previous cases within both your organization and networks.
Evidence tab. Highlights user-selected variant pathogenicity, ACMG class (for a sequence or a genomic variant), and interpretation notes.
Expandable Variant activity panel (right). Records variant-level user activities, such as tagging a variant, adding comments or evidence notes, or editing the evidence graph. Variant activity panel pops up upon clicking the Activities button.

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