ClinVar Miner

List of variants reported as pathogenic for partial deletion of the short arm of chromosome 16 by GeneReviews

Included ClinVar conditions (6):

16p13.11 microdeletion syndrome
Chromosome 16p12.1 deletion syndrome, 520kb
Chromosome 16p12.2-p11.2 deletion syndrome
Distal 16p11.2 microdeletion syndrome
Proximal 16p11.2 microdeletion syndrome
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion

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: 1

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HGVS	dbSNP	gnomAD frequency
16p11.2 recurrent region (BP4-BP5)

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