ClinVar Miner

List of intergenic variants reported as uncertain significance by ISCA site 4

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
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HGVS dbSNP
GRCh38/hg38 11q21(chr11:96607634-96937648)x1
GRCh38/hg38 1p35.2(chr1:30116821-30696608)x1
GRCh38/hg38 2q32.3(chr2:193305897-193900771)x3
GRCh38/hg38 3p26.1(chr3:5480153-6021420)x3
GRCh38/hg38 3p26.3(chr3:1780588-2045586)x3
GRCh38/hg38 4p15.31(chr4:19656960-20172216)x3
GRCh38/hg38 4q25(chr4:107398371-107562376)x3
GRCh38/hg38 5q21.2-21.3(chr5:104482674-105488260)x1
GRCh38/hg38 5q21.2-21.3(chr5:104482674-105488260)x3
GRCh38/hg38 7q11.22(chr7:70891025-71072442)x3
GRCh38/hg38 8q24.22(chr8:131149372-131527501)x3
GRCh38/hg38 9p23(chr9:10648009-11435662)x1
GRCh38/hg38 9p24.2(chr9:2324333-2501030)x1
GRCh38/hg38 Xq21.33(chrX:97669841-98038562)x0
GRCh38/hg38 Xq27.3(chrX:144251509-144887684)x2
GRCh38/hg38 Yq11.221(chrY:15445716-16977713)x3

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