ClinVar Miner

List of intergenic variants reported as pathogenic for not provided

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Gene type:
ClinVar version:
Total variants: 12
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GRCh37/hg19 1q31.1(chr1:188620903-188928487)x1
GRCh37/hg19 1q31.1-31.2(chr1:190622633-191184941)x1
GRCh37/hg19 Xp22.33(chrX:168546-1358900)x1
GRCh37/hg19 Xp22.33(chrX:168546-1616945)x1
GRCh37/hg19 Xp22.33(chrX:168546-781139)x1
GRCh37/hg19 Xp22.33(chrX:482532-1460944)x1
GRCh37/hg19 Xp22.33(chrX:502307-1234634)x1
GRCh37/hg19 Yq11.23-12(chrY:28792268-58883690)x0
Single allele rs527236214

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