List of intergenic variants reported as likely pathogenic for chromosomal 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
NCBI36/hg18 17p13.1(chr17:6853665-8107394)x4
NC_000023.10:g.(152882907_152991027)del
NC_000023.10:g.(152886255_152976269)del
NC_000023.10:g.(152982350_153041544)del

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