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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5712994mobile element insertion2nstd211human GRCh38 chr7: 128,716,672-128,716,672 , GRCh37.p13 chr7: 128,356,726-128,356,726 GARIN1B
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5489101copy number variation1nstd206human GRCh38 chr7: 128,719,138-128,721,591 , GRCh37.p13 chr7: 128,359,192-128,361,645 GARIN1B
    nsv5410236mobile element insertion1nstd206human GRCh38 chr7: 128,716,655-128,716,655 , GRCh37.p13 chr7: 128,356,709-128,356,709 GARIN1B
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5108201mobile element insertion1nstd203human GRCh38 chr7: 128,716,655-128,716,672 , GRCh37.p13 chr7: 128,356,709-128,356,726 GARIN1B
    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
    nsv4968739copy number variation1nstd200human GRCh38 chr7: 128,553,668-128,746,707 , GRCh37.p13 chr7: 128,193,722-128,386,761 , RPS10P15, 9 more genes
    nsv4958255copy number variation1nstd200human GRCh38 chr7: 128,728,807-128,731,670 , GRCh37.p13 chr7: 128,368,861-128,371,724 GARIN1B
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4820513copy number variation1nstd200human GRCh37 chr7: 128,368,861-128,371,724 , GRCh38.p12 chr7: 128,728,807-128,731,670 GARIN1B
    nsv4706634copy number variation1nstd195human GRCh37 chr7: 128,368,858-128,368,859 , GRCh38.p12 chr7: 128,728,804-128,728,805 GARIN1B
    nsv4675620copy number variation1nstd102humanPathogenic GRCh37 chr7: 109,251,060-159,119,707 , GRCh38.p12 chr7: 109,611,003-159,327,017 RPL26P23, ST13P17, 887 more genes
    nsv4675607copy number variation1nstd102humanUncertain significance GRCh37 chr7: 128,084,932-128,354,937 , GRCh38.p12 chr7: 128,444,878-128,714,883 RNA5SP242, RPS10P15, 10 more genes
    nsv4675275copy number variation1nstd102humanUncertain significance GRCh37 chr7: 128,038,651-128,369,771 , GRCh38.p12 chr7: 128,398,597-128,729,717 RNA5SP242, CICP14, 13 more genes
    nsv4543770insertion1nstd166human GRCh37.p13 chr7: 128,356,709-128,356,709 , GRCh38.p12 chr7: 128,716,655-128,716,655 GARIN1B
    nsv4457011copy number variation1nstd102humanUncertain significance GRCh37 chr7: 127,999,644-128,465,294 , GRCh38.p12 chr7: 128,359,590-128,825,240 IMPDH1, GARIN1A, 20 more genes
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