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Items: 1 to 20 of 251

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099231copy number variation1nstd231human GRCh38.p12 chr1: 149,962,894-151,006,586 , GRCh37 chr1: 149,934,818-150,979,062 ARNT, CTSK, 48 more genes
    nsv7056211inversion1nstd229human GRCh38 chr1: 143,881,700-152,159,818 , GRCh37.p13 chr1|NW_003871055.3: 697,113-7,283,150 , PDIA3P1, 333 more genes
    nsv7044458inversion1nstd229human GRCh38 chr1: 150,355,899-155,246,175 , GRCh37.p13 chr1: 150,440,214-155,215,966 LCE2C, MUC1, 254 more genes
    nsv7042502inversion1nstd229human GRCh38 chr1: 150,301,267-155,517,761 , GRCh37.p13 chr1: 150,440,214-155,487,552 LINGO4, CELF3, 268 more genes
    nsv6642108copy number variation1nstd229human GRCh38 chr1: 150,760,547-150,857,506 , GRCh37.p13 chr1: 150,733,023-150,829,982 LOC100132571, CTSS, 4 more genes
    nsv6641764copy number variation1nstd229human GRCh38 chr1: 150,761,787-151,277,656 , GRCh37.p13 chr1: 150,734,263-151,250,132 VPS72, RPS29P29, 30 more genes
    nsv6542656inversion1nstd223human GRCh38 chr1: 150,871,321-150,871,908 , GRCh37.p13 chr1: 150,843,797-150,844,384 ARNT
    nsv6535608inversion1nstd223human GRCh38 chr1: 150,859,107-150,859,661 , GRCh37.p13 chr1: 150,831,583-150,832,137 ARNT
    nsv6335375copy number variation1nstd223human GRCh38 chr1: 150,811,791-150,812,578 , GRCh37.p13 chr1: 150,784,267-150,785,054 RNU6-1309P, ARNT
    nsv6333911copy number variation1nstd223human GRCh38 chr1: 150,847,761-150,870,903 , GRCh37.p13 chr1: 150,820,237-150,843,379 ARNT
    nsv6328897copy number variation1nstd223human GRCh38 chr1: 150,855,403-150,856,635 , GRCh37.p13 chr1: 150,827,879-150,829,111 ARNT
    nsv6326578copy number variation1nstd223human GRCh38 chr1: 150,861,243-150,862,922 , GRCh37.p13 chr1: 150,833,719-150,835,398 ARNT
    nsv6310678copy number variation4nstd102humanUncertain significance GRCh37 chr1: 149,895,434-156,851,434 , GRCh38.p12 chr1: 149,923,542-156,881,642 PRPF3, KHDC4, 352 more genes
    nsv6292438mobile element insertion1nstd186human GRCh37 chr1: 150,791,353-150,791,404 , GRCh38.p12 chr1: 150,818,877-150,818,928 ARNT
    nsv6245258mobile element insertion1nstd215human GRCh38 chr1: 150,873,997-150,873,997 , GRCh37.p13 chr1: 150,846,473-150,846,473 ARNT
    nsv6133734copy number variation1nstd213human GRCh37 chr1: 150,350,000-154,440,001 , GRCh38.p12 chr1: 150,377,524-154,467,525 , MCL1, 216 more genes
    nsv6133733copy number variation1nstd213human GRCh37 chr1: 149,980,000-151,620,001 , GRCh38.p12 chr1: 150,008,051-151,647,525 CTSK, MCL1, 80 more genes
    nsv6133732copy number variation1nstd213human GRCh37 chr1: 149,750,000-153,310,001 , GRCh38.p12 chr1: 149,778,444-153,337,525 , CTSK, 183 more genes
    nsv6133499copy number variation1nstd213human GRCh37 chr1: 149,880,000-153,720,001 , GRCh38.p12 chr1: 149,908,448-153,747,525 , CTSK, 198 more genes
    nsv5887303copy number variation1nstd209human GRCh38 chr1: 150,853,114-150,854,789 , GRCh37.p13 chr1: 150,825,590-150,827,265 ARNT
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