New ClinVar graphical display

Maps clinically significant variants by gene and position! ClinVar is a freely accessible, public archive of reports of the relationships between human variations and phenotypes, with supporting evidence at NLM/NCBI. To help you access your variants of interest quickly, ClinVar is introducing an all-new visualization tool in the search results. This graphical display provides an … Continue reading New ClinVar graphical display →
Source: NCBI Insights - Category: Databases & Libraries Authors: Tags: What's New ClinVar Human variant data Variation Source Type: news