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Items: 1 to 20 of 27

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3907001copy number variation1nstd102humanBenign GRCh37 chr11: 8,958,492-8,964,938 , GRCh38.p12 chr11: 8,936,945-8,943,391 ASCL3
    nsv3892291copy number variation1nstd102humanBenign GRCh37 chr11: 8,958,903-8,964,938 , GRCh38.p12 chr11: 8,937,356-8,943,391 ASCL3
    nsv3894757copy number variation1nstd102humanBenign GRCh37 chr11: 8,959,020-8,964,938 , GRCh38.p12 chr11: 8,937,473-8,943,391 ASCL3
    nsv3888507copy number variation1nstd102humannot provided GRCh37 chr11: 8,959,020-8,964,938 , GRCh38 chr11: 8,937,473-8,943,391 ASCL3
    nsv3898491copy number variation1nstd102humanconflicting data from submitters GRCh37 chr11: 8,959,136-8,964,546 , GRCh38.p12 chr11: 8,937,589-8,942,999 ASCL3
    esv3648557copy number variation1estd216humannot provided GRCh37 chr11: 8,959,020-8,964,938 , GRCh38.p12 chr11: 8,937,473-8,943,391 ASCL3
    nsv3903880copy number variation1nstd102humanBenign GRCh37 chr11: 8,948,615-8,964,938 , GRCh38.p12 chr11: 8,927,068-8,943,391 ASCL3, C11orf16
    nsv3899570copy number variation1nstd102humanBenign GRCh37 chr11: 8,953,850-8,964,938 , GRCh38.p12 chr11: 8,932,303-8,943,391 ASCL3, C11orf16
    nsv3904925copy number variation1nstd102humanLikely benign GRCh37 chr11: 8,959,136-8,968,875 , GRCh38.p12 chr11: 8,937,589-8,947,328 ASCL3, TMEM9B
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 ASCL3, LOC105376598, 2842 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 ASCL3, RTN3, 2833 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 ASCL3, IGHMBP2, 2829 more genes
    nsv3898926copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-37,698,540 , GRCh38.p12 chr11: 230,615-37,676,990 ASCL3, OR51L1, 771 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 ASCL3, BGLT3, 723 more genes
    nsv3906221copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-31,995,219 , GRCh38.p12 chr11: 230,615-31,973,673 ASCL3, PCNAP4, 688 more genes
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 ASCL3, OR52Q1P, 630 more genes
    nsv3894525copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-25,584,362 , GRCh38.p12 chr11: 230,615-25,562,816 ASCL3, SDHCP4, 620 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 ASCL3, TRIM22, 546 more genes
    nsv3898948copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-17,099,213 , GRCh38.p12 chr11: 230,615-17,077,666 ASCL3, MTND5P21, 506 more genes
    nsv4350476copy number variation1nstd102humanPathogenic GRCh37 chr11: 193,146-12,643,136 , GRCh38.p12 chr11: 193,146-12,621,589 ASCL3, KRTAP5-3, 457 more genes
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