ClinVar Miner

List of intergenic variants reported as pathogenic by Geschwind lab,University of California Los Angeles

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
Download table as spreadsheet
HGVS dbSNP
NC_000001.9:g.144943150_146293282del1350133
NC_000001.9:g.144967972_146293282dup
NC_000001.9:g.144970465_146293282dup
NC_000001.9:g.145119261_146293282dup
NC_000005.8:g.175492445_177359136del1866692
NC_000015.8:g.19359417_26208861dup
NC_000015.8:g.19359417_30302218del10942802
NC_000015.8:g.21200233_26762141dup
NC_000015.8:g.26762141_30302218del3540078
NC_000015.8:g.28723577_30322604del1599028
NC_000016.8:g.29554843_30085308del530466
NC_000016.8:g.29554843_30085308dup
NC_000017.9:g.14039002_15411904dup
NC_000017.9:g.14040467_15411904del1371438
NC_000017.9:g.14040467_15411904dup
NC_000022.9:g.17257787_18686993dup
NC_000022.9:g.17257787_19792353dup
NC_000022.9:g.17266915_21751058dup
NC_000022.9:g.21309897_23340746dup
NC_000022.9:g.21995356_23326630dup

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.