VarSome Clinical offers the option to the user to generate a clinical report of specific variants in PDF or Word format.
Variant reporting works on a sample level, i.e. you can report multiple variants belonging to the same sample, but you can't report one variant of the sample A and another of the sample B within the same report.
In the Variant Table page, you can either select one variant at a time just by clicking on it or you can select multiple variants at once (mass selection) by holding Ctrl and clicking on each variant you wish to include to your list and then click on the "Select for export" 
option. On the left, click on the arrow icon 
to see the list of variants selected for export, and then choose "Generate Report".
Then, you will be directed to the following screen:
The form we provide as a template to create your report is completely customizable, where all section tables can be edited according to the user's needs (see more about that here). The final report layout you choose to generate will be saved for future use.
What is more, by clicking on the 
icon, a Report widgets menu will be shown, with the following options:
- Analysis information: General information including sample name, predicted gender, phenotypes, and diseases.
- Content area: Field to write content-related information of the analysis.
- All variants' information: Table with all selected variant's information.
- Variant information: Mutation identification, followed by its classification and a short description of the variant. More information is included containing HGVS notation, related gene, exon, variant type, rs ID, zygosity, frequency, and coverage.
- Variant references: List of scientific papers referring to a specific variant.
- Gene information: Disease-related information from CGD, about the gene containing a specific variant.
- Related drugs (if applicable): Information regarding the drug-gene interactions from DGIdb, and other data resources.
- PMKB info (if applicable): Information about the gene containing a specific variant, retrieved from PMKB database.
- CIVIC info (if applicable): Information about mutations shown to predict response to targeted therapy from CIViC database.
- GHR info (if applicable): gene information from GHR.
- Clinical Trials info (if applicable): Information about related clinical studies from AACT database [1].
You can "drag and drop" one by one all the information you wish to include in the report.
