ClinVar Miner

List of intergenic variants reported as uncertain significance by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
Download table as spreadsheet
HGVS dbSNP
GRCh37/hg19 1q44(chr1:244229113-244452045)x3
GRCh37/hg19 Xp22.33(chrX:176426-677595)x3
GRCh37/hg19 Xp22.33(chrX:193483-571339)x3
GRCh37/hg19 Xp22.33(chrX:225816-809572)x3
GRCh37/hg19 Xp22.33(chrX:460130-1008586)x3
GRCh37/hg19 Xp22.33(chrX:524370-591887)x3
GRCh37/hg19 Xp22.33(chrX:597797-643697)x3
GRCh37/hg19 Xp22.33(chrX:605776-1252566)x4
GRCh37/hg19 Xp22.33(chrX:614422-1347337)x3
GRCh37/hg19 Yp11.32(chrY:564422-1297337)x3
GRCh38/hg38 11q21(chr11:94324359-94366689)x1
GRCh38/hg38 12q21.31(chr12:85584352-85784283)x1
GRCh38/hg38 14q24.3(chr14:75398690-75425417)x3
GRCh38/hg38 17p11.2(chr17:18219346-18225106)x3
GRCh38/hg38 21q22.3(chr21:46019502-46096306)x3
GRCh38/hg38 2p25.3(chr2:50661-140943)x1
GRCh38/hg38 3p26.2(chr3:3195997-3503302)x1
GRCh38/hg38 3q12.3(chr3:102481295-102566368)x3
GRCh38/hg38 4q25(chr4:109355081-109404907)x1
GRCh38/hg38 4q32.1(chr4:157385121-157506916)x1
GRCh38/hg38 5q13.1(chr5:68319663-68479180)x3
GRCh38/hg38 5q21.1(chr5:100746003-100793223)x1

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.