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Items: 19

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    Number of Variants: 19

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 PTPN5, FAUP4, 2031 more genes
    nsv3901577copy number variation1nstd102humanPathogenic GRCh37 chr11: 18,536,224-31,923,308 , GRCh38.p12 chr11: 18,514,677-31,901,762 PTPN5, LOC105376588, 137 more genes
    nsv3919437copy number variation1nstd102humanPathogenic GRCh37 chr11: 17,926,636-19,696,051 , NCBI36 chr11: 17,883,212-19,652,627 , GRCh38 chr11: 17,905,089-19,674,505 PTPN5, CSRP3-AS1, 55 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 PTPN5, LOC105376598, 2842 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 PTPN5, RTN3, 2833 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 PTPN5, IGHMBP2, 2829 more genes
    nsv3898926copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-37,698,540 , GRCh38.p12 chr11: 230,615-37,676,990 PTPN5, OR51L1, 771 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 PTPN5, BGLT3, 723 more genes
    nsv3906221copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-31,995,219 , GRCh38.p12 chr11: 230,615-31,973,673 PTPN5, PCNAP4, 688 more genes
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 PTPN5, OR52Q1P, 630 more genes
    nsv3894525copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-25,584,362 , GRCh38.p12 chr11: 230,615-25,562,816 PTPN5, SDHCP4, 620 more genes
    nsv4674824copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,053,978-34,732,891 , GRCh38.p12 chr11: 11,032,431-34,711,344 PTPN5, SNORA88, 305 more genes
    nsv3912558copy number variation1nstd102humanPathogenic GRCh37 chr11: 446,754-18,926,289 , GRCh38 chr11: 446,754-18,904,742 , NCBI36 chr11: 436,754-18,882,865 PTPN5, TRIM22, 546 more genes
    nsv4675502copy number variation1nstd102humanPathogenic GRCh37 chr11: 13,970,757-27,565,888 , GRCh38.p12 chr11: 13,949,210-27,544,341 PTPN5, MRGPRX5P, 171 more genes
    nsv7093841copy number variation1nstd102humanUncertain significance GRCh37 chr11: 18,418,390-19,204,313 , GRCh38.p12 chr11: 18,396,843-19,182,766 PTPN5, UEVLD, 25 more genes
    nsv6314200copy number variation1nstd102humanUncertain significance GRCh37 chr11: 18,482,438-18,792,764 , GRCh38.p12 chr11: 18,460,891-18,771,217 PTPN5, LDHAL6A, 11 more genes
    nsv3921634copy number variation1nstd102humanUncertain significance NCBI36 chr11: 18,504,345-20,726,247 , GRCh38 chr11: 18,526,222-20,748,125 , GRCh37 chr11: 18,547,769-20,769,671 PTPN5, NELL1, 41 more genes
    nsv5380720copy number variation1nstd102humanUncertain significance GRCh37 chr11: 17,552,691-19,213,995 , GRCh38.p12 chr11: 17,531,144-19,192,448 PTPN5, USH1C, 53 more genes
    nsv6637654copy number variation1nstd102humanUncertain significance GRCh37 chr11: 17,784,556-18,797,650 , GRCh38.p12 chr11: 17,763,009-18,776,103 PTPN5, LOC112268073, 37 more genes
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