List of intergenic variants reported as likely benign by Medical Cytogenetics and Molecular Genetics Laboratory, IRCCS Istituto Auxologico Italiano

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
NC_000004.11:g.31744797_31975862del231066
NC_000008.11:g.90692712_90718088dup
NC_000023.10:g.151638056_151743864del105809
NC_000023.10:g.74772380_74826319del53940

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