ClinVar: updates to support classifications of both germline and somatic variants

Topics

ClinVar · Germline variants · Somatic mutations · Variant annotation · oncogenicity classification · clinical impact classification · human genetic variants · disease-variant relationships · public database · genomic database · batch submission · submission API · online submission forms · ClinVar XML files · ClinVar VCF files · tab-delimited files · variant aggregation · ClinVar VCV pages · clinical testing laboratories · Cancer genomics · genomic testing · transparency in genomic testing · patient care · NCBI · variant curation · somatic variant interpretation · germline variant interpretation