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Items: 1 to 20 of 190

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5924810copy number variation1nstd209human GRCh38 chr7: 128,751,153-128,751,215 , GRCh37.p13 chr7: 128,391,207-128,391,269 CALU
    nsv5914456copy number variation1nstd209human GRCh38 chr7: 128,499,704-128,999,795 , GRCh37.p13 chr7: 128,139,758-128,639,849 , KCP, 25 more genes
    nsv5911338copy number variation1nstd209human GRCh38 chr7: 128,499,612-128,999,703 , GRCh37.p13 chr7: 128,139,666-128,639,757 , CICP14, 25 more genes
    nsv5699468mobile element insertion1nstd211human GRCh38 chr7: 128,762,233-128,762,233 , GRCh37.p13 chr7: 128,402,287-128,402,287 CALU
    nsv5579803copy number variation1nstd207human GRCh38 chr7: 128,751,153-128,751,215 , GRCh37.p13 chr7: 128,391,207-128,391,269 CALU
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5487987copy number variation1nstd206human GRCh38 chr7: 128,751,156-128,751,216 , GRCh37.p13 chr7: 128,391,210-128,391,270 CALU
    nsv5485476copy number variation1nstd206human GRCh38 chr7: 128,748,870-128,749,894 , GRCh37.p13 chr7: 128,388,924-128,389,948 CALU
    nsv5406656mobile element insertion1nstd206human GRCh38 chr7: 128,762,233-128,762,284 , GRCh37.p13 chr7: 128,402,287-128,402,338 CALU
    nsv5345777translocation1nstd200human GRCh37 chr7: 128,409,674-128,409,674 , GRCh37 chr2: 63,835,510-63,835,510 , GRCh38.p12 chr7: 128,769,620-128,769,620 , GRCh38.p12 chr2: 63,608,376-63,608,376 CALU
    nsv5345631translocation1nstd200human GRCh37 chr7: 128,411,528-128,411,528 , GRCh37 chr2: 63,835,512-63,835,512 , GRCh38.p12 chr7: 128,771,474-128,771,474 , GRCh38.p12 chr2: 63,608,378-63,608,378 OPN1SW, CALU
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5115254mobile element insertion1nstd203human GRCh38 chr7: 128,762,218-128,762,233 , GRCh37.p13 chr7: 128,402,272-128,402,287 CALU
    nsv5114375mobile element insertion1nstd203human GRCh38 chr7: 128,757,567-128,757,582 , GRCh37.p13 chr7: 128,397,621-128,397,636 CALU
    nsv5110089mobile element insertion1nstd203human GRCh38 chr7: 128,768,847-128,768,868 , GRCh37.p13 chr7: 128,408,901-128,408,922 CALU
    nsv5102994mobile element insertion1nstd203human GRCh38 chr7: 128,759,415-128,759,432 , GRCh37.p13 chr7: 128,399,469-128,399,486 CALU, RN7SL81P
    nsv5102365mobile element insertion1nstd203human GRCh38 chr7: 128,752,679-128,752,688 , GRCh37.p13 chr7: 128,392,733-128,392,742 CALU
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4968741copy number variation1nstd200human GRCh38 chr7: 128,746,207-128,746,924 , GRCh37.p13 chr7: 128,386,261-128,386,978 CALU
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