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Items: 1 to 20 of 119

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3881060copy number variation1nstd102humanBenign GRCh37 chr1: 3,362,256-3,417,211 , GRCh38.p12 chr1: 3,445,692-3,500,647 ARHGEF16, MEGF6
    nsv3883141copy number variation1nstd102humanBenign GRCh37 chr1: 3,362,256-3,416,173 , GRCh38.p12 chr1: 3,445,692-3,499,609 ARHGEF16, MEGF6
    nsv3885908copy number variation1nstd102humanBenign GRCh37 chr1: 3,389,727-3,423,467 , GRCh38.p12 chr1: 3,473,163-3,506,903 ARHGEF16, MEGF6
    nsv3881167copy number variation1nstd102humanBenign GRCh37 chr1: 3,393,037-3,423,467 , GRCh38.p12 chr1: 3,476,473-3,506,903 ARHGEF16, MEGF6
    nsv3875036copy number variation1nstd102humanBenign GRCh37 chr1: 3,393,037-3,418,462 , GRCh38.p12 chr1: 3,476,473-3,501,898 ARHGEF16, MEGF6
    nsv3888942copy number variation1nstd102humanBenign GRCh37 chr1: 3,393,037-3,417,211 , GRCh38.p12 chr1: 3,476,473-3,500,647 ARHGEF16, MEGF6
    nsv6290672copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,466-17,525,065 , GRCh38.p12 chr1: 914,086-17,198,570 ARHGEF16, RPL9P11, 466 more genes
    nsv3900501copy number variation1nstd102humanPathogenic GRCh38 chr1: 3,006,193-17,688,934 , GRCh37 chr1: 2,922,757-18,015,429 , NCBI36 chr1: 2,912,617-17,888,016 ARHGEF16, MFFP1, 364 more genes
    nsv3873030copy number variation1nstd102humanPathogenic GRCh37 chr1: 746,608-15,077,159 , GRCh38.p12 chr1: 811,228-14,750,663 ARHGEF16, RN7SL451P, 376 more genes
    nsv3888433copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-12,699,337 , GRCh38.p12 chr1: 82,154-12,639,316 ARHGEF16, AURKAIP1, 356 more genes
    nsv4436105copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-11,784,118 , GRCh38.p12 chr1: 82,154-11,724,061 ARHGEF16, PARK7, 325 more genes
    nsv3899046copy number variation1nstd102humanPathogenic GRCh38 chr1: 844,347-12,470,133 , GRCh37 chr1: 779,727-12,530,188 , NCBI36 chr1: 769,590-12,452,775 ARHGEF16, PRKCZ-DT, 315 more genes
    nsv6637093copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,467-12,448,956 , GRCh38.p12 chr1: 914,087-12,388,897 ARHGEF16, VWA1, 311 more genes
    nsv6315409copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,466-10,258,804 , GRCh38.p12 chr1: 914,086-10,198,746 ARHGEF16, VAMP3, 245 more genes
    nsv4436631copy number variation1nstd102humanPathogenic GRCh37 chr1: 554,375-9,779,842 , GRCh38.p12 chr1: 618,995-9,719,784 ARHGEF16, LINC02606, 253 more genes
    nsv3913374copy number variation1nstd102humanPathogenic NCBI36 chr1: 4,737-8,767,973 , GRCh37.p13 chr1: 14,874-8,845,386 , GRCh38.p12 chr1: 14,874-8,785,327 ARHGEF16, LOC105378593, 252 more genes
    nsv3907841copy number variation1nstd102humanPathogenic GRCh37 chr1: 837,491-9,616,363 , GRCh38 chr1: 902,111-9,556,305 , NCBI36 chr1: 827,354-9,538,950 ARHGEF16, PRKCZ-AS1, 224 more genes
    nsv3890178copy number variation1nstd102humanPathogenic NCBI36 chr1: 839,329-9,549,767 , GRCh37 chr1: 849,466-9,627,180 , GRCh38 chr1: 914,086-9,567,122 ARHGEF16, ANKRD65, 224 more genes
    nsv3909850copy number variation1nstd102humanPathogenic GRCh37 chr1: 846,680-9,389,984 , GRCh38 chr1: 911,300-9,329,925 , NCBI36 chr1: 836,543-9,312,571 ARHGEF16, LOC105378590, 221 more genes
    nsv3889222copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,466-8,901,938 , GRCh38.p12 chr1: 914,086-8,841,879 ARHGEF16, PLEKHG5, 205 more genes
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