ClinVar Miner

List of intergenic variants reported as uncertain significance by Clinical Cytogenomics Laboratory,Laboratory for Precision Diagnostics, University of Washington

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 17
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GRCh37/hg19 10p12.31(chr10:19417181-19834795)x1
GRCh37/hg19 10q25.1(chr10:107371918-107854441)x3
GRCh37/hg19 13q21.31(chr13:62515937-63487629)x4
GRCh37/hg19 16q11.2(chr16:44565757-44895960)x3
GRCh37/hg19 5p14.3(chr5:20208626-20669942)x3
GRCh37/hg19 8p23.3(chr8:847144-1375610)x1
GRCh37/hg19 8q21.3(chr8:89383727-90028363)x3
GRCh37/hg19 8q23.2-23.3(chr8:111417315-112383323)x1
GRCh37/hg19 Xp11.4(chrX:39031508-39794957)x3
GRCh37/hg19 Xp22.33(chrX:1581361-1971039)x3
GRCh37/hg19 Xp22.33(chrX:2058563-2473906)x3
GRCh37/hg19 Xp22.33(chrX:489911-728395)x3
GRCh37/hg19 Xp22.33(chrX:578382-1021508)x3
GRCh37/hg19 Xp22.33(chrX:60814-537179)x3
GRCh37/hg19 Xp22.33(chrX:829150-1422943)x3
GRCh37/hg19 Xp22.33(chrX:851541-1389532)x3
GRCh37/hg19 Xp22.33(chrX:949989-1613434)x3

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