List of intergenic variants reported as pathogenic for benign neoplasm

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

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
46;XX;ins(5;6)(p13;p24p25)dn
46;XY;inv(6)(p22q13)dn
46;XY;t(7;13)(p15.3;q14.1)dn

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