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: 15
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HGVS dbSNP gnomAD frequency
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 17p11.2(chr17:18219346-18225106)x3
GRCh38/hg38 2p25.3(chr2:50661-140943)x1
GRCh38/hg38 4q25(chr4:109355081-109404907)x1
GRCh38/hg38 4q32.1(chr4:157385121-157506916)x1

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