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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 or dbVar as appropriate. Please contact us if you have any questions.
dbSNP and dbVar variant positions are now based GRCh38.

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