You can use the Import Variant tool to import all the variants that are contained in a VCF file into your Geneticist Assistant database. If the VCF file contains the pathogenicity and pathogenicity status for the variants, variants comments and/or variant artifact types, then you can also import this information. If the VCF file’s INFO fields do not contain this information, then you can still use the tool to import the variants that are contained in the file, but then you can manually set the pathogenicity and/or pathogenicity status for the variants, as well as add a comment for the variants and/or set the artifact types. For either situation, this means that if multiple variants have the same pathogenicity and/or artifact type for a panel group, you do not have to set the pathogenicity of each variant individually. Instead, you can use this tool to set the same pathogenicity and/or artifact type for all the variants at once.