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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
    nsv7051994inversion1nstd229human GRCh38 chr1: 1,135,450-1,178,690 , GRCh37.p13 chr1: 1,070,830-1,114,070 MIR200B, TTLL10-AS1, 4 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
    nsv7040598inversion1nstd229human GRCh38 chr1: 1,016,054-1,174,806 , GRCh37.p13 chr1: 951,434-1,110,186 MIR200A, LINC01342, 9 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
    nsv6656142copy number variation1nstd229human GRCh38 chr1: 838,653-1,166,615 , GRCh37.p13 chr1: 774,033-1,101,995 LINC01128, SAMD11, 21 more genes
    nsv6640639copy number variation1nstd229human GRCh38 chr1: 1,158,973-1,175,599 , GRCh37.p13 chr1: 1,094,353-1,110,979 TTLL10-AS1, MIR200B, 3 more genes
    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
    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
    nsv6315409copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,466-10,258,804 , GRCh38.p12 chr1: 914,086-10,198,746 VAMP3, CTNNBIP1, 245 more genes
    nsv6315371copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,466-2,518,608 , GRCh38.p12 chr1: 914,086-2,587,169 LINC01786, MMP23A, 96 more genes
    nsv6315344copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,466-4,183,006 , GRCh38.p12 chr1: 914,086-4,122,946 DFFB, LOC105378604, 136 more genes
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