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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
    nsv7099018copy number variation1nstd102humanPathogenic GRCh37 chr1: 1-2,580,976 , GRCh38.p12 chr1: 10,001-2,649,537 DVL1, LOC100129534, 148 more genes
    nsv7096012copy number variation1nstd102humanUncertain significance GRCh37 chr1: 980,719-1,168,648 , GRCh38.p12 chr1: 1,045,339-1,233,268 SDF4, TNFRSF18, 13 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
    nsv6657199copy number variation1nstd229human GRCh38 chr1: 926,615-1,239,899 , GRCh37.p13 chr1: 861,995-1,175,279 TTLL10-AS1, MIR200B, 21 more genes
    nsv6640893copy number variation1nstd229human GRCh38 chr1: 1,207,339-1,207,761 , GRCh37.p13 chr1: 1,142,719-1,143,141 TNFRSF18
    nsv6640857copy number variation1nstd229human GRCh38 chr1: 1,186,001-1,207,400 , GRCh37.p13 chr1: 1,121,381-1,142,780 TTLL10, TNFRSF18
    nsv6640796copy number variation1nstd229human GRCh38 chr1: 1,206,435-1,212,803 , GRCh37.p13 chr1: 1,141,815-1,148,183 TNFRSF18, TNFRSF4
    nsv6640792copy number variation1nstd229human GRCh38 chr1: 1,202,997-1,209,322 , GRCh37.p13 chr1: 1,138,377-1,144,702 TNFRSF18
    nsv6640543copy number variation1nstd229human GRCh38 chr1: 1,156,215-1,304,768 , GRCh37.p13 chr1: 1,091,595-1,240,148 MIR429, TTLL10, 14 more genes
    nsv6640137copy number variation1nstd229human GRCh38 chr1: 1,130,518-1,270,042 , GRCh37.p13 chr1: 1,065,898-1,205,422 TTLL10, MIR429, 10 more genes
    nsv6639644copy number variation1nstd229human GRCh38 chr1: 1,089,392-1,302,400 , GRCh37.p13 chr1: 1,024,772-1,237,780 B3GALT6, C1QTNF12, 15 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
    nsv6637018copy number variation1nstd102humanUncertain significance GRCh37 chr1: 1,129,319-1,264,880 , GRCh38.p12 chr1: 1,193,939-1,329,500 SNORD167, TAS1R3, 15 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
    nsv6636416copy number variation1nstd102humanUncertain significance GRCh37 chr1: 849,467-1,174,365 , GRCh38.p12 chr1: 914,087-1,238,985 RNF223, SAMD11, 24 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
    nsv6625341copy number variation1nstd224human GRCh37 chr1: 1,079,261-1,158,357 , GRCh38.p12 chr1: 1,143,881-1,222,977 TNFRSF4, TNFRSF18, 7 more genes
    nsv6625333copy number variation1nstd224human GRCh37 chr1: 1,018,704-1,179,816 , GRCh38.p12 chr1: 1,083,324-1,244,436 SDF4, LINC01342, 10 more genes
    nsv6625098copy number variation1nstd224human GRCh37 chr1: 1,138,913-1,149,109 , GRCh38.p12 chr1: 1,203,533-1,213,729 TNFRSF4, TNFRSF18
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