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Items: 1 to 20 of 252

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077759inversion1nstd229human GRCh38 chr12: 102,103,848-102,127,536 , GRCh37.p13 chr12: 102,497,626-102,521,314 PARPBP, NUP37
    nsv7075858inversion1nstd229human GRCh38 chr12: 102,016,372-102,210,884 , GRCh37.p13 chr12: 102,410,150-102,604,662 PMCH, WASHC3, 2 more genes
    nsv7074674inversion1nstd229human GRCh38 chr12: 100,072,817-104,989,567 , GRCh37.p13 chr12: 100,466,595-105,383,345 SYCP3, GOLGA2P5, 84 more genes
    nsv7068655inversion1nstd229human GRCh38 chr12: 102,059,119-102,307,599 , GRCh37.p13 chr12: 102,452,897-102,701,377 WASHC3, PMCH, 5 more genes
    nsv7068612inversion1nstd229human GRCh38 chr12: 100,083,131-104,989,539 , GRCh37.p13 chr12: 100,476,909-105,383,317 EID3, RNU6-1068P, 84 more genes
    nsv6934850copy number variation1nstd229human GRCh38 chr12: 102,132,864-102,358,197 , GRCh37.p13 chr12: 102,526,642-102,751,975 LOC100418882, PMCH, 3 more genes
    nsv6931503copy number variation1nstd229human GRCh38 chr12: 102,142,094-102,146,605 , GRCh37.p13 chr12: 102,535,872-102,540,383 PARPBP
    nsv6931167copy number variation1nstd229human GRCh38 chr12: 101,984,162-102,207,248 , GRCh37.p13 chr12: 102,377,940-102,601,026 NUP37, PARPBP, 2 more genes
    nsv6929767copy number variation1nstd229human GRCh38 chr12: 102,122,357-102,132,472 , GRCh37.p13 chr12: 102,516,135-102,526,250 PARPBP
    nsv6929502copy number variation1nstd229human GRCh38 chr12: 102,183,168-102,213,855 , GRCh37.p13 chr12: 102,576,946-102,607,633 PARPBP, PMCH
    nsv6929001copy number variation1nstd229human GRCh38 chr12: 102,119,074-102,156,410 , GRCh37.p13 chr12: 102,512,852-102,550,188 PARPBP, NUP37
    nsv6926321copy number variation1nstd229human GRCh38 chr12: 102,151,779-102,161,129 , GRCh37.p13 chr12: 102,545,557-102,554,907 PARPBP
    nsv6926158copy number variation1nstd229human GRCh38 chr12: 102,144,964-102,149,172 , GRCh37.p13 chr12: 102,538,742-102,542,950 PARPBP
    nsv6924768copy number variation1nstd229human GRCh38 chr12: 102,159,805-102,183,807 , GRCh37.p13 chr12: 102,553,583-102,577,585 PARPBP
    nsv6924294copy number variation1nstd229human GRCh38 chr12: 102,140,824-102,149,743 , GRCh37.p13 chr12: 102,534,602-102,543,521 PARPBP
    nsv6924143copy number variation1nstd229human GRCh38 chr12: 102,173,155-102,187,621 , GRCh37.p13 chr12: 102,566,933-102,581,399 PARPBP
    nsv6922635copy number variation1nstd229human GRCh38 chr12: 96,115,345-104,800,221 , GRCh37.p13 chr12: 96,509,123-105,193,999 RNY1P16, CHST11, 121 more genes
    nsv6921966copy number variation1nstd229human GRCh38 chr12: 102,173,832-102,297,133 , GRCh37.p13 chr12: 102,567,610-102,690,911 RN7SL793P, PMCH, 3 more genes
    nsv6920514copy number variation1nstd229human GRCh38 chr12: 102,152,686-102,160,533 , GRCh37.p13 chr12: 102,546,464-102,554,311 PARPBP
    nsv6621485copy number variation1nstd224human GRCh37 chr12: 102,558,304-102,576,340 , GRCh38.p12 chr12: 102,164,526-102,182,562 PARPBP
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