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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5925156copy number variation1nstd209human GRCh38 chr12: 8,656,198-8,656,804 , GRCh37.p13 chr12: 8,808,794-8,809,400 MFAP5
    nsv5546700insertion1nstd206human GRCh38 chr12: 8,656,638-8,656,648 , GRCh37.p13 chr12: 8,809,234-8,809,244 MFAP5
    nsv5507264copy number variation1nstd206human GRCh38 chr12: 8,656,214-8,656,827 , GRCh37.p13 chr12: 8,808,810-8,809,423 MFAP5
    nsv5495384copy number variation1nstd206human GRCh38 chr12: 8,652,366-8,654,814 , GRCh37.p13 chr12: 8,804,962-8,807,410 MFAP5
    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
    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
    nsv4972126copy number variation1nstd200human GRCh38 chr12: 8,656,793-8,659,364 , GRCh37.p13 chr12: 8,809,389-8,811,960 MFAP5
    nsv4972125copy number variation1nstd200human GRCh38 chr12: 8,656,521-8,661,893 , GRCh37.p13 chr12: 8,809,117-8,814,489 MFAP5
    nsv4972124copy number variation1nstd200human GRCh38 chr12: 8,652,373-8,654,826 , GRCh37.p13 chr12: 8,804,969-8,807,422 MFAP5
    nsv4882300inversion1nstd200human GRCh37 chr12: 6,338,820-22,046,498 , GRCh38.p12 chr12: 6,229,654-21,893,564 , LOC105369686, 414 more genes
    nsv4847432copy number variation1nstd200human GRCh37 chr12: 8,809,117-8,814,489 , GRCh38.p12 chr12: 8,656,521-8,661,893 MFAP5
    nsv4839564copy number variation1nstd200human GRCh37 chr12: 8,809,389-8,811,960 , GRCh38.p12 chr12: 8,656,793-8,659,364 MFAP5
    nsv4836486copy number variation1nstd200human GRCh37 chr12: 8,808,786-8,809,390 , GRCh38.p12 chr12: 8,656,190-8,656,794 MFAP5
    nsv4674941copy number variation1nstd102humanPathogenic GRCh37 chr12: 274,676-37,869,301 , GRCh38.p12 chr12: 165,510-37,475,499 LOC105376675, ATF7IP, 682 more genes
    nsv4668144copy number variation1nstd186human GRCh37 chr12: 8,804,914-8,807,410 , GRCh38.p12 chr12: 8,652,318-8,654,814 MFAP5
    nsv4617647copy number variation1nstd183human GRCh37 chr12: 8,798,860-8,804,175 , GRCh38.p12 chr12: 8,646,264-8,651,579 MFAP5
    nsv4616824copy number variation1nstd183human GRCh37 chr12: 8,488,721-9,625,223 , GRCh38.p12 chr12: 8,336,125-9,472,627 , BTG1P1, 43 more genes
    nsv4615835copy number variation1nstd183human GRCh37 chr12: 8,804,914-8,807,410 , GRCh38.p12 chr12: 8,652,318-8,654,814 MFAP5
    nsv4504066mobile element insertion1nstd166human GRCh37.p13 chr12: 8,797,994-8,797,994 , GRCh38.p12 chr12: 8,645,398-8,645,398 MFAP5
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