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Items: 1 to 20 of 141

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7041767inversion1nstd229human GRCh38 chr2: 7,061,548-10,183,852 , GRCh37.p13 chr2: 7,201,679-10,323,978 LINC00298, KLF11, 52 more genes
    nsv6675393copy number variation1nstd229human GRCh38 chr2: 10,059,194-10,066,622 , GRCh37.p13 chr2: 10,199,321-10,206,749 CYS1
    nsv6675279copy number variation1nstd229human GRCh38 chr2: 10,011,501-10,506,700 , GRCh37.p13 chr2: 10,151,628-10,646,826 ODC1, HPCAL1, 11 more genes
    nsv6672311copy number variation1nstd229human GRCh38 chr2: 10,073,500-10,073,552 , GRCh37.p13 chr2: 10,213,627-10,213,679 CYS1
    nsv6672305copy number variation1nstd229human GRCh38 chr2: 10,060,397-10,063,812 , GRCh37.p13 chr2: 10,200,524-10,203,939 CYS1
    nsv6669168copy number variation1nstd229human GRCh38 chr2: 10,065,632-10,074,984 , GRCh37.p13 chr2: 10,205,759-10,215,111 CYS1
    nsv6667086copy number variation1nstd229human GRCh38 chr2: 10,047,295-10,133,315 , GRCh37.p13 chr2: 10,187,422-10,273,442 CYS1, RRM2, 1 more genes
    nsv6666576copy number variation1nstd229human GRCh38 chr2: 6,592,339-11,769,396 , GRCh37.p13 chr2: 6,732,471-11,909,522 RN7SKP112, LOC101929861, 103 more genes
    nsv6665766copy number variation1nstd229human GRCh38 chr2: 10,068,568-10,075,966 , GRCh37.p13 chr2: 10,208,695-10,216,093 CYS1
    nsv6663823copy number variation1nstd229human GRCh38 chr2: 10,010,915-10,140,233 , GRCh37.p13 chr2: 10,151,042-10,280,360 LOC112268412, KLF11, 3 more genes
    nsv6660139copy number variation1nstd229human GRCh38 chr2: 10,048,301-10,097,600 , GRCh37.p13 chr2: 10,188,428-10,237,727 KLF11, CYS1
    nsv6636993copy number variation1nstd102humanUncertain significance GRCh37 chr2: 10,192,689-10,462,223 , GRCh38.p12 chr2: 10,052,562-10,322,097 LOC101929691, CYS1, 6 more genes
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 LOC105374455, RN7SL674P, 504 more genes
    nsv6345747copy number variation1nstd223human GRCh38 chr2: 10,065,632-10,074,978 , GRCh37.p13 chr2: 10,205,759-10,215,105 CYS1
    nsv6341329copy number variation1nstd223human GRCh38 chr2: 10,060,394-10,063,808 , GRCh37.p13 chr2: 10,200,521-10,203,935 CYS1
    nsv6339652copy number variation1nstd223human GRCh38 chr2: 10,010,915-10,140,233 , GRCh37.p13 chr2: 10,151,042-10,280,360 KLF11-DT, KLF11, 3 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6290643copy number variation1nstd102humanUncertain significance GRCh37 chr2: 8,935,077-15,722,794 , GRCh38.p12 chr2: 8,794,947-15,582,670 PPIAP60, LOC105373431, 95 more genes
    nsv6290363copy number variation1nstd102humanUncertain significance GRCh37 chr2: 9,717,186-12,013,065 , GRCh38.p12 chr2: 9,577,057-11,872,939 RNU4-73P, CYS1, 56 more genes
    nsv6134471copy number variation1nstd213human GRCh37 chr2: 9,710,000-10,900,001 , GRCh38.p12 chr2: 9,569,871-10,759,875 HPCAL1, ODC1, 26 more genes
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