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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5725594mobile element insertion1nstd211human GRCh38 chr12: 8,516,081-8,516,081 , GRCh37.p13 chr12: 8,668,677-8,668,677 CLEC4D
    nsv5506440copy number variation1nstd206human GRCh38 chr12: 8,513,752-8,513,909 , GRCh37.p13 chr12: 8,666,348-8,666,505 CLEC4D
    nsv5503359copy number variation1nstd206human GRCh38 chr12: 8,508,894-8,512,500 , GRCh37.p13 chr12: 8,661,490-8,665,096 CLEC4D, SUPT4H1P2
    nsv5323122inversion1nstd204human GRCh37.p13 chr12: 6,338,815-22,046,498 , GRCh38.p13 chr12: 6,229,649-21,893,564 , A2M, 414 more genes
    nsv5029743inversion1nstd200human GRCh38 chr12: 7,297,013-15,308,349 , GRCh37.p13 chr12: 7,449,609-15,461,283 , MIR1244-4, 259 more genes
    nsv4974317copy number variation1nstd200human GRCh38 chr12: 8,513,752-8,513,909 , GRCh37.p13 chr12: 8,666,348-8,666,505 CLEC4D
    nsv4974316copy number variation1nstd200human GRCh38 chr12: 8,482,988-8,890,234 , GRCh37.p13 chr12: 8,635,584-9,042,830 MFAP5, SUPT4H1P2, 10 more genes
    nsv4974311copy number variation1nstd200human GRCh38 chr12: 8,295,898-8,571,996 , GRCh37.p13 chr12: 8,448,494-8,724,592 SUPT4H1P2, RPL15P17, 14 more genes
    nsv4974308copy number variation1nstd200human GRCh38 chr12: 8,126,743-8,525,672 , GRCh37.p13 chr12: 8,279,339-8,678,268 LINC00937, CLEC4D, 23 more genes
    nsv4972120copy number variation1nstd200human GRCh38 chr12: 8,520,389-8,521,987 , GRCh37.p13 chr12: 8,672,985-8,674,583 CLEC4D
    nsv4972119copy number variation1nstd200human GRCh38 chr12: 8,508,894-8,512,500 , GRCh37.p13 chr12: 8,661,490-8,665,096 CLEC4D, SUPT4H1P2
    nsv4882300inversion1nstd200human GRCh37 chr12: 6,338,820-22,046,498 , GRCh38.p12 chr12: 6,229,654-21,893,564 , LOC105369686, 414 more genes
    nsv4841551copy number variation1nstd200human GRCh37 chr12: 8,448,494-8,724,592 , GRCh38.p12 chr12: 8,295,898-8,571,996 SNRPCP7, CLEC4E, 14 more genes
    nsv4836376copy number variation1nstd200human GRCh37 chr12: 8,661,490-8,665,096 , GRCh38.p12 chr12: 8,508,894-8,512,500 CLEC4D, SUPT4H1P2
    nsv4835774copy number variation1nstd200human GRCh37 chr12: 8,666,348-8,666,505 , GRCh38.p12 chr12: 8,513,752-8,513,909 CLEC4D
    nsv4831856copy number variation1nstd200human GRCh37 chr12: 8,672,985-8,674,583 , GRCh38.p12 chr12: 8,520,389-8,521,987 CLEC4D
    nsv4681960copy number variation1nstd102humanPathogenic GRCh37 chr12: 8,608,708-8,765,363 , GRCh38.p12 chr12: 8,456,112-8,612,767 CLEC4E, AICDA, 6 more genes
    nsv4674941copy number variation1nstd102humanPathogenic GRCh37 chr12: 274,676-37,869,301 , GRCh38.p12 chr12: 165,510-37,475,499 LOC105376675, ATF7IP, 682 more genes
    nsv4616824copy number variation1nstd183human GRCh37 chr12: 8,488,721-9,625,223 , GRCh38.p12 chr12: 8,336,125-9,472,627 , BTG1P1, 43 more genes
    nsv4616796copy number variation1nstd183human GRCh37 chr12: 8,529,392-8,773,126 , GRCh38.p12 chr12: 8,376,796-8,620,530 OR7E148P, LOC105369645, 10 more genes
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