List of intergenic variants reported as pathogenic by Liping Wei Laboratory, Peking University

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: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
15q11.2-12duplication
15q13.3duplication
15q25.3duplication
1q42.2deletion
22q11.21deletion
2q37.3deletion
7q31.32deletion
7q32.3duplication
7q35 duplication
9p24.1deletion

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.