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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5496577copy number variation1nstd206human GRCh38 chr11: 20,883,122-21,568,664 , GRCh37.p13 chr11: 20,904,668-21,590,210 NELL1, LOC100631258, 3 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5256856copy number variation1nstd204human GRCh38.p13 chr11: 20,975,601-21,071,700 , GRCh37.p13 chr11: 20,997,147-21,093,246 RNA5SP336, NELL1
    nsv5249700copy number variation1nstd204human GRCh38.p13 chr11: 20,976,248-21,003,355 , GRCh37.p13 chr11: 20,997,794-21,024,901 NELL1, RNA5SP336
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4675502copy number variation1nstd102humanPathogenic GRCh37 chr11: 13,970,757-27,565,888 , GRCh38.p12 chr11: 13,949,210-27,544,341 MRGPRX5P, LDHC, 171 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4674824copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,053,978-34,732,891 , GRCh38.p12 chr11: 11,032,431-34,711,344 SNORA88, LINC02729, 305 more genes
    nsv4528950copy number variation1nstd166human GRCh37.p13 chr11: 20,673,999-21,062,000 , GRCh38.p12 chr11: 20,652,453-21,040,454 , NELL1, 3 more genes
    nsv4490950mobile element insertion1nstd166human GRCh37.p13 chr11: 21,022,055-21,022,055 , GRCh38.p12 chr11: 21,000,509-21,000,509 RNA5SP336, NELL1
    nsv4455902copy number variation1nstd102humanUncertain significance GRCh37 chr11: 20,792,281-21,073,130 , GRCh38.p12 chr11: 20,770,735-21,051,584 LOC105376585, NELL1, 1 more genes
    nsv3922794copy number variation1nstd102humanPathogenic GRCh37 chr11: 20,101,020-34,485,543 , GRCh38 chr11: 20,079,474-34,463,996 , NCBI36 chr11: 20,057,596-34,442,119 LOC107984419, LINC02758, 150 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
    nsv3906221copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-31,995,219 , GRCh38.p12 chr11: 230,615-31,973,673 PCNAP4, LIN7C, 688 more genes
    nsv3901577copy number variation1nstd102humanPathogenic GRCh37 chr11: 18,536,224-31,923,308 , GRCh38.p12 chr11: 18,514,677-31,901,762 LOC105376588, LOC105376585, 137 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 more genes
    nsv3898926copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-37,698,540 , GRCh38.p12 chr11: 230,615-37,676,990 OR51L1, OR52V1P, 771 more genes
    nsv3894525copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-25,584,362 , GRCh38.p12 chr11: 230,615-25,562,816 SDHCP4, SWAP70, 620 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 LOC105376598, OSBPL9P2, 2842 more genes
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