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Items: 1 to 20 of 803

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147339copy number variation1nstd232human GRCh38.p12 chr1: 1,312,147-1,312,224 , GRCh37.p13 chr1: 1,247,527-1,247,604 INTS11, PUSL1, 1 more genes
    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
    nsv7044349inversion1nstd229human GRCh38 chr1: 1,282,566-1,352,764 , GRCh37.p13 chr1: 1,217,946-1,288,144 PUSL1, MIR6808, 10 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
    nsv6641293copy number variation1nstd229human GRCh38 chr1: 1,311,620-1,318,369 , GRCh37.p13 chr1: 1,247,000-1,253,749 PUSL1, INTS11, 1 more genes
    nsv6641158copy number variation1nstd229human GRCh38 chr1: 1,310,792-1,310,910 , GRCh37.p13 chr1: 1,246,172-1,246,290 PUSL1, INTS11, 1 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
    nsv6636292copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,467-2,972,435 , GRCh38.p12 chr1: 914,087-3,055,871 LOC105378602, LOC105378599, 108 more genes
    nsv6635030copy number variation1nstd227human GRCh38.p12 chr1: 1,303,959-1,311,592 , GRCh37 chr1: 1,239,339-1,246,972 INTS11, ACAP3, 3 more genes
    nsv6625602copy number variation1nstd224human GRCh37 chr1: 1,226,757-1,268,687 , GRCh38.p12 chr1: 1,291,377-1,333,307 TAS1R3, ACAP3, 8 more genes
    nsv6625599copy number variation1nstd224human GRCh37 chr1: 1,220,954-1,268,482 , GRCh38.p12 chr1: 1,285,574-1,333,102 SCNN1D, INTS11, 7 more genes
    nsv6625554copy number variation1nstd224human GRCh37 chr1: 1,222,895-1,249,193 , GRCh38.p12 chr1: 1,287,515-1,313,813 SCNN1D, INTS11, 5 more genes
    nsv6625552copy number variation1nstd224human GRCh37 chr1: 1,222,218-1,246,022 , GRCh38.p12 chr1: 1,286,838-1,310,642 SCNN1D, INTS11, 5 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
    nsv6315170copy number variation1nstd102humanPathogenic GRCh37 chr1: 834,101-7,930,605 , GRCh38.p12 chr1: 898,721-7,870,545 PRDM16-DT, CAMTA1-AS1, 186 more genes
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