This proposal seeks to add a new 'ranges' input parameter to find-subject-dx-implications and find-subject-tx-implications. Currently, subject phenotype operations require specified variants or haplotypes as input. This new parameter will simplify the return of clinically relevant variants from a given region. Specifically: [1] Add a 'ranges' input parameter to find-subject-dx-implications and find-subject-tx-implications; [2] The ranges parameter will be defined just as it is used in find-subject-variants; [3] If 'ranges' are submitted, the response is subject's variants in specified ranges that have associated diagnostic or therapeutic implications.