Figure 1.
NCBI Sequence Viewer (SV) is the graphical component of many NCBI pages and is configured to display data appropriate to the resource page. (A) SV located on an NCBI gene record page. Brown labels indicate tracks for sequence, gene annotation, and RNA-seq data. (B) SV located on an NCBI SNP record page. Brown labels indicate tracks for gene annotation, RefSNPs, Clinical (ClinVar), missense, and frameshift variants. A marker is automatically placed over the variant described on the page.
