Human Variation: Annotation and Submit Batch Data with Clinical Impact
Submit multiple variants using HGVS nomenclature with an opportunity to identify their clinical relevance
Your submissions will be processed into ClinVar
and assigned ClinVar accessions (SCV). Novel variant locations will also be accessioned in dbSNP
as appropriate. Please contact us
if you have any questions.
dbSNP and dbVar variant positions are now based GRCh38.