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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974522insertion1nstd209human GRCh38 chr12: 14,684,563-14,684,563 , GRCh37.p13 chr12: 14,837,497-14,837,497 GUCY2C, C12orf60
    nsv5921487copy number variation1nstd209human GRCh38 chr12: 14,615,448-14,662,490 , GRCh37.p13 chr12: 14,768,382-14,815,424 GUCY2C, C12orf60, 1 more genes
    nsv5865678copy number variation1nstd209human GRCh38 chr12: 14,649,868-14,655,177 , GRCh37.p13 chr12: 14,802,802-14,808,111 GUCY2C, C12orf60
    nsv5861945copy number variation1nstd209human GRCh38 chr12: 14,626,141-14,628,840 , GRCh37.p13 chr12: 14,779,075-14,781,774 GUCY2C, C12orf60
    nsv5861738copy number variation1nstd209human GRCh38 chr12: 14,641,748-14,646,417 , GRCh37.p13 chr12: 14,794,682-14,799,351 GUCY2C, C12orf60
    nsv5859233copy number variation1nstd209human GRCh38 chr12: 14,648,018-14,650,651 , GRCh37.p13 chr12: 14,800,952-14,803,585 C12orf60, GUCY2C
    nsv5858482copy number variation1nstd209human GRCh38 chr12: 14,639,498-14,641,497 , GRCh37.p13 chr12: 14,792,432-14,794,431 C12orf60, GUCY2C
    nsv5857852copy number variation1nstd209human GRCh38 chr12: 14,647,918-14,661,788 , GRCh37.p13 chr12: 14,800,852-14,814,722 GUCY2C, C12orf60
    nsv5855121copy number variation1nstd209human GRCh38 chr12: 14,614,990-14,619,266 , GRCh37.p13 chr12: 14,767,924-14,772,200 GUCY2C, C12orf60, 1 more genes
    nsv5853838copy number variation1nstd209human GRCh38 chr12: 14,649,968-14,653,377 , GRCh37.p13 chr12: 14,802,902-14,806,311 C12orf60, GUCY2C
    nsv5849544copy number variation1nstd209human GRCh38 chr12: 14,619,517-14,635,297 , GRCh37.p13 chr12: 14,772,451-14,788,231 GUCY2C, C12orf60, 1 more genes
    nsv5847616copy number variation1nstd209human GRCh38 chr12: 14,649,768-14,654,377 , GRCh37.p13 chr12: 14,802,702-14,807,311 C12orf60, GUCY2C
    nsv5696103mobile element insertion2nstd211human GRCh38 chr12: 14,657,453-14,657,453 , GRCh37.p13 chr12: 14,810,387-14,810,387 GUCY2C, C12orf60
    nsv5592915copy number variation1nstd207human GRCh38 chr12: 14,697,011-14,697,067 , GRCh37.p13 chr12: 14,849,945-14,850,001 C12orf60, GUCY2C
    nsv5551043insertion1nstd206human GRCh38 chr12: 14,642,272-14,642,272 , GRCh37.p13 chr12: 14,795,206-14,795,206 C12orf60, GUCY2C
    nsv5419508mobile element insertion1nstd206human GRCh38 chr12: 14,657,453-14,657,504 , GRCh37.p13 chr12: 14,810,387-14,810,438 GUCY2C, C12orf60
    nsv5338928translocation1nstd200human GRCh37 chr12: 14,795,368-14,795,368 , GRCh37 chr12: 14,795,206-14,795,206 , GRCh38.p12 chr12: 14,642,272-14,642,272 , GRCh38.p12 chr12: 14,642,434-14,642,434 C12orf60, GUCY2C
    nsv5329332translocation1nstd204human GRCh37.p13 chr12: 14,795,206-14,795,206 , GRCh37.p13 chr12: 14,795,368-14,795,368 , GRCh38.p13 chr12: 14,642,272-14,642,272 , GRCh38.p13 chr12: 14,642,434-14,642,434 GUCY2C, C12orf60
    nsv5323122inversion1nstd204human GRCh37.p13 chr12: 6,338,815-22,046,498 , GRCh38.p13 chr12: 6,229,649-21,893,564 , A2M, 414 more genes
    nsv5196283mobile element insertion1nstd203human GRCh38 chr12: 14,695,216-14,695,229 , GRCh37.p13 chr12: 14,848,150-14,848,163 C12orf60, GUCY2C
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