ClinVar database usage
In ClinVar database,using variation viewer tool, after uploading .vcf file of identified mutations, all mutations are displaying in bottom resultant table, apart from those which are present in uploaded .vcf file. But I want to see only those mutations which are present in my .vcf file. How to do that? What settings I have to do in Variation viewer tool?
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rucha.wadapurkar •
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Looks like you have also posted on ResearchGate:
Can you point me to the exact page where you upload the VCF?