ClinVar Miner

List of variants reported as not provided for partial deletion of the short arm of chromosome 16

Included ClinVar conditions (6):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
GRCh37/hg19 16p11.2(chr16:29651706-30193525)x1
GRCh37/hg19 16p13.11(chr16:15154115-16276115)
GRCh37/hg19 16p13.11-12.3(chr16:15494600-18141051)x1
Single allele

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