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Items: 1 to 20 of 951

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148127copy number variation1nstd102humanUncertain significance GRCh37 chr7: 10,973,263-14,669,896 , GRCh38.p12 chr7: 10,933,636-14,630,271 LOC105375162, LOC105375156, 33 more genes
    nsv7056782inversion1nstd229human GRCh38 chr7: 11,728,530-11,757,950 , GRCh37.p13 chr7: 11,768,157-11,797,576 THSD7A
    nsv7056409inversion1nstd229human GRCh38 chr7: 11,659,536-11,659,568 , GRCh37.p13 chr7: 11,699,163-11,699,195 THSD7A
    nsv7054063inversion1nstd229human GRCh38 chr7: 7,723,636-12,911,662 , GRCh37.p13 chr7: 7,763,267-12,951,287 NXPH1, CCNB2P1, 50 more genes
    nsv7049984inversion1nstd229human GRCh38 chr7: 11,159,456-12,799,960 , GRCh37.p13 chr7: 11,199,083-12,839,585 THSD7A, LOC105375156, 17 more genes
    nsv7049910inversion1nstd229human GRCh38 chr7: 11,601,031-11,817,569 , GRCh37.p13 chr7: 11,640,658-11,857,195 THSD7A
    nsv7047585inversion1nstd229human GRCh38 chr7: 11,549,908-11,736,698 , GRCh37.p13 chr7: 11,589,535-11,776,325 LOC105375151, THSD7A
    nsv7045602inversion1nstd229human GRCh38 chr7: 11,447,561-11,447,613 , GRCh37.p13 chr7: 11,487,188-11,487,240 THSD7A
    nsv7045188inversion1nstd229human GRCh38 chr7: 11,734,479-11,752,519 , GRCh37.p13 chr7: 11,774,106-11,792,145 THSD7A
    nsv7045164inversion1nstd229human GRCh38 chr7: 11,830,745-11,891,921 , GRCh37.p13 chr7: 11,870,371-11,931,547 THSD7A
    nsv7045075inversion1nstd229human GRCh38 chr7: 11,499,919-11,503,457 , GRCh37.p13 chr7: 11,539,546-11,543,084 THSD7A
    nsv7043971inversion1nstd229human GRCh38 chr7: 11,578,233-11,578,286 , GRCh37.p13 chr7: 11,617,860-11,617,913 LOC105375151, THSD7A
    nsv7040883inversion1nstd229human GRCh38 chr7: 11,731,126-12,171,021 , GRCh37.p13 chr7: 11,770,753-12,210,647 THRAP3P3, THSD7A
    nsv7039997inversion1nstd229human GRCh38 chr7: 11,435,976-11,740,653 , GRCh37.p13 chr7: 11,475,603-11,780,280 LOC105375151, THSD7A
    nsv6817616copy number variation1nstd229human GRCh38 chr7: 11,565,287-11,570,686 , GRCh37.p13 chr7: 11,604,914-11,610,313 LOC105375151, THSD7A
    nsv6817347copy number variation1nstd229human GRCh38 chr7: 11,337,201-11,653,300 , GRCh37.p13 chr7: 11,376,828-11,692,927 LOC105375151, THSD7A
    nsv6817043copy number variation1nstd229human GRCh38 chr7: 11,491,001-11,499,900 , GRCh37.p13 chr7: 11,530,628-11,539,527 THSD7A
    nsv6817024copy number variation1nstd229human GRCh38 chr7: 11,707,396-11,707,815 , GRCh37.p13 chr7: 11,747,023-11,747,442 THSD7A
    nsv6816913copy number variation1nstd229human GRCh38 chr7: 11,363,571-11,407,860 , GRCh37.p13 chr7: 11,403,198-11,447,487 THSD7A
    nsv6816413copy number variation1nstd229human GRCh38 chr7: 11,629,193-11,631,955 , GRCh37.p13 chr7: 11,668,820-11,671,582 THSD7A
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