ClinVar annotations now available in NCBI Genome Browsers

Do you need to know which of the many NCBI dbSNP variants annotated near your region of interest are likely to be functionally or clinically significant? Figure it out with the track labelled  ‘ClinVar variants with precise endpoints’, available on sequence display viewers at NCBI, including the Genome Data Viewer (GDV) and Variation Viewer! This track shows variation … Continue reading ClinVar annotations now available in NCBI Genome Browsers →
Source: NCBI Insights - Category: Databases & Libraries Authors: Tags: Quick Tips ClinVar Genome Data Viewer (GDV) Variation Viewer Source Type: news