List of intergenic variants reported as uncertain significance for hematologic disorder

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: 4

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HGVS	dbSNP	gnomAD frequency
46;XX;inv(2)(q13q14.2)
46;XX;t(6;20)(q25.1;p13)dn
46;XY;t(16;20)(q23.1;p11.22)
NC_000017.11:g.44393555C>T	rs2048710914

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