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Items: 1 to 20 of 899

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137045copy number variation1nstd102humanPathogenic GRCh37 chr1: 536,777-6,012,896 , GRCh38.p12 chr1: 601,397-5,952,836 MIR200B, LOC105378608, 172 more genes
    nsv7099170copy number variation1nstd231human GRCh38.p12 chr1: 1,558,660-2,125,257 , GRCh37 chr1: 1,494,040-2,056,696 CDK11B, GABRD, 23 more genes
    nsv7099018copy number variation1nstd102humanPathogenic GRCh37 chr1: 1-2,580,976 , GRCh38.p12 chr1: 10,001-2,649,537 DVL1, LOC100129534, 148 more genes
    nsv7050245inversion1nstd229human GRCh38 chr1: 1,663,824-1,702,798 , GRCh37.p13 chr1: 1,595,263-1,634,237 CDK11A, MMP23A, 2 more genes
    nsv7044270inversion1nstd229human GRCh38 chr1: 1,133,718-2,842,494 , GRCh37.p13 chr1: 1,069,098-2,759,059 LOC105378586, MIR6726, 91 more genes
    nsv7040524inversion1nstd229human GRCh38 chr1: 1,668,899-1,673,768 , GRCh37.p13 chr1: 1,600,338-1,605,207 LOC100288379, SLC35E2B
    nsv6644268copy number variation1nstd229human GRCh38 chr1: 1,684,901-1,748,200 , GRCh37.p13 chr1: 1,616,340-1,679,639 MMP23A, SLC35E2A, 4 more genes
    nsv6644260copy number variation1nstd229human GRCh38 chr1: 1,682,013-1,682,041 , GRCh37.p13 chr1: 1,613,452-1,613,480 SLC35E2B
    nsv6644216copy number variation1nstd229human GRCh38 chr1: 1,684,501-1,748,000 , GRCh37.p13 chr1: 1,615,940-1,679,439 SLC35E2A, LOC100129381, 4 more genes
    nsv6644142copy number variation1nstd229human GRCh38 chr1: 1,681,972-1,685,381 , GRCh37.p13 chr1: 1,613,411-1,616,820 SLC35E2B
    nsv6643788copy number variation1nstd229human GRCh38 chr1: 1,689,201-1,734,300 , GRCh37.p13 chr1: 1,620,640-1,665,739 MMP23A, SLC35E2B, 3 more genes
    nsv6637093copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,467-12,448,956 , GRCh38.p12 chr1: 914,087-12,388,897 VWA1, CEP104, 311 more genes
    nsv6636801copy number variation1nstd102humanPathogenic GRCh37 chr1: 1,335,011-2,302,755 , GRCh38.p12 chr1: 1,399,631-2,371,316 SSU72, MRPL20, 44 more genes
    nsv6636661copy number variation1nstd102humanUncertain significance GRCh37 chr1: 1,130,311-2,397,177 , GRCh38.p12 chr1: 1,194,931-2,465,738 ATAD3C, ACAP3, 69 more genes
    nsv6636292copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,467-2,972,435 , GRCh38.p12 chr1: 914,087-3,055,871 LOC105378602, LOC105378599, 108 more genes
    nsv6625851copy number variation1nstd224human GRCh37 chr1: 1,597,351-1,647,858 , GRCh38.p12 chr1: 1,665,912-1,716,419 MMP23A, LOC100288379, 2 more genes
    nsv6625849copy number variation1nstd224human GRCh37 chr1: 1,572,310-1,680,219 , GRCh38.p12 chr1: 1,636,948-1,748,780 CDK11B, MMP23A, 6 more genes
    nsv6625848copy number variation1nstd224human GRCh37 chr1: 1,562,091-1,664,124 , GRCh38.p12 chr1: 1,626,711-1,732,685 CDK11B, MMP23B, 6 more genes
    nsv6625782copy number variation1nstd224human GRCh37 chr1: 1,597,351-1,647,780 , GRCh38.p12 chr1: 1,665,912-1,716,341 CDK11A, MMP23A, 2 more genes
    nsv6625778copy number variation8nstd224human GRCh37 chr1: 1,572,310-1,611,995 , GRCh38.p12 chr1: 1,636,948-1,680,556 LOC100288379, CDK11B, 1 more genes
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