U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 691

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5381304copy number variation2nstd102humanUncertain significance GRCh37 chr1: 948,954-1,284,445 , GRCh38.p12 chr1: 1,013,574-1,349,065 LOC100288175, UBE2J2, 28 more genes
    nsv5381061copy number variation2nstd102humanUncertain significance GRCh37 chr1: 1,146,915-1,168,668 , GRCh38.p12 chr1: 1,211,535-1,233,288 B3GALT6, TNFRSF4, 1 more genes
    nsv5299725copy number variation1nstd204human GRCh38.p13 chr1: 995,894-1,230,896 , GRCh37.p13 chr1: 931,274-1,166,276 SDF4, RPL39P12, 16 more genes
    nsv5213610copy number variation1nstd204human GRCh38.p13 chr1: 1,193,268-1,221,063 , GRCh37.p13 chr1: 1,128,648-1,156,443 TNFRSF18, TNFRSF4, 2 more genes
    nsv5208305copy number variation1nstd204human GRCh38.p13 chr1: 890,901-1,634,500 , GRCh37.p13 chr1: 826,281-1,569,876 , PLEKHN1, 62 more genes
    nsv5203371copy number variation1nstd204human GRCh38.p13 chr1: 934,001-1,382,300 , GRCh37.p13 chr1: 869,381-1,317,680 AGRN, UBE2J2, 38 more genes
    nsv4905945copy number variation1nstd200human GRCh38 chr1: 1,209,926-1,238,178 , GRCh37.p13 chr1: 1,145,306-1,173,558 TNFRSF4, B3GALT6, 1 more genes
    nsv4894238copy number variation1nstd200human GRCh38 chr1: 1,208,408-1,219,768 , GRCh37.p13 chr1: 1,143,788-1,155,148 SDF4, TNFRSF4
    nsv4894237copy number variation1nstd200human GRCh38 chr1: 1,184,149-1,244,759 , GRCh37.p13 chr1: 1,119,529-1,180,139 TNFRSF4, TNFRSF18, 4 more genes
    nsv4894236copy number variation1nstd200human GRCh38 chr1: 1,159,957-1,276,804 , GRCh37.p13 chr1: 1,095,337-1,212,184 UBE2J2, TTLL10, 10 more genes
    nsv4782543copy number variation1nstd200human GRCh37 chr1: 1,148,402-1,148,773 , GRCh38.p12 chr1: 1,213,022-1,213,393 TNFRSF4
    nsv4772082copy number variation1nstd200human GRCh37 chr1: 1,119,529-1,180,139 , GRCh38.p12 chr1: 1,184,149-1,244,759 SDF4, TNFRSF4, 4 more genes
    nsv4772081copy number variation1nstd200human GRCh37 chr1: 1,095,337-1,212,184 , GRCh38.p12 chr1: 1,159,957-1,276,804 LINC01786, MIR200B, 10 more genes
    nsv4769317copy number variation1nstd102humanPathogenic GRCh37 chr1: 753,462-1,717,335 , GRCh38.p12 chr1: 818,082-1,785,896 MMP23B, DVL1, 76 more genes
    nsv4728693copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,466-2,033,256 , GRCh38.p12 chr1: 914,086-2,101,817 SDF4, GNB1-DT, 80 more genes
    nsv4728279copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 849,466-1,806,659 , GRCh38.p12 chr1: 914,086-1,875,220 CDK11B, DVL1, 70 more genes
    nsv4728263copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,466-1,976,788 , GRCh38.p12 chr1: 914,086-2,045,349 VWA1, MRPL20, 78 more genes
    nsv4728187copy number variation1nstd102humanPathogenic GRCh37 chr1: 1-5,592,835 , GRCh38.p12 chr1: 10,001-5,532,775 UBE2J2, MRPL20, 196 more genes
    nsv4685972copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 762,080-7,309,686 , GRCh38.p12 chr1: 826,700-7,249,626 CDK11B, DFFB, 184 more genes
    nsv4683680copy number variation1nstd102humanUncertain significance GRCh37 chr1: 948,934-1,249,188 , GRCh38.p12 chr1: 1,013,554-1,313,808 MIR6727, LOC105378948, 24 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center