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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3870758copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 4,816,199-4,825,153 , GRCh38 chr7: 4,776,568-4,785,522 AP5Z1
    nsv3906094copy number variation1nstd102humanBenign GRCh37 chr7: 4,830,379-4,854,998 , GRCh38.p12 chr7: 4,790,748-4,815,367 AP5Z1, RADIL
    nsv3884863copy number variation1nstd102humanUncertain significance GRCh37 chr7: 4,827,785-4,834,026 , GRCh38 chr7: 4,788,154-4,794,395 AP5Z1, MIR4656
    nsv3903089copy number variation1nstd102humanBenign GRCh37 chr7: 4,821,300-4,854,998 , GRCh38.p12 chr7: 4,781,669-4,815,367 AP5Z1, RADIL, 1 more genes
    nsv3896538copy number variation1nstd102humanBenign GRCh37 chr7: 4,823,392-4,845,701 , GRCh38.p12 chr7: 4,783,761-4,806,070 AP5Z1, RADIL, 1 more genes
    nsv3905291copy number variation1nstd102humanBenign GRCh37 chr7: 4,823,971-4,845,248 , GRCh38.p12 chr7: 4,784,340-4,805,617 AP5Z1, RADIL, 1 more genes
    nsv3905860copy number variation1nstd102humanBenign GRCh37 chr7: 4,823,971-4,842,603 , GRCh38.p12 chr7: 4,784,340-4,802,972 AP5Z1, MIR4656, 1 more genes
    nsv3906768copy number variation1nstd102humanBenign GRCh37 chr7: 4,824,622-4,841,553 , GRCh38.p12 chr7: 4,784,991-4,801,922 AP5Z1, RADIL, 1 more genes
    nsv3906844copy number variation1nstd102humanBenign GRCh37 chr7: 4,798,726-4,854,998 , GRCh38.p12 chr7: 4,759,095-4,815,367 AP5Z1, FOXK1, 2 more genes
    nsv3895145copy number variation1nstd102humanBenign GRCh37 chr7: 4,821,332-4,876,055 , GRCh38.p12 chr7: 4,781,701-4,836,424 AP5Z1, SNORD165, 2 more genes
    nsv3905285copy number variation1nstd102humanBenign GRCh37 chr7: 4,824,622-4,876,055 , GRCh38.p12 chr7: 4,784,991-4,836,424 AP5Z1, RADIL, 2 more genes
    nsv3894297copy number variation1nstd102humanBenign GRCh37 chr7: 4,799,694-4,845,701 , GRCh38.p12 chr7: 4,760,063-4,806,070 AP5Z1, RADIL, 2 more genes
    nsv3895135copy number variation1nstd102humanBenign GRCh37 chr7: 4,821,300-4,855,994 , GRCh38.p12 chr7: 4,781,669-4,816,363 AP5Z1, RADIL, 1 more genes
    nsv3898657copy number variation1nstd102humanBenign GRCh37 chr7: 4,798,726-4,830,979 , GRCh38.p12 chr7: 4,759,095-4,791,348 AP5Z1, MIR4656, 1 more genes
    nsv3909428copy number variation1nstd102humanBenign GRCh37 chr7: 4,821,300-4,839,882 , GRCh38.p12 chr7: 4,781,669-4,800,251 AP5Z1, RADIL, 1 more genes
    nsv3896681copy number variation1nstd102humanBenign GRCh37 chr7: 4,821,300-4,839,265 , GRCh38.p12 chr7: 4,781,669-4,799,634 AP5Z1, MIR4656, 1 more genes
    nsv6289843copy number variation1nstd102humanUncertain significance GRCh37 chr7: 4,736,454-4,860,123 , GRCh38.p12 chr7: 4,696,823-4,820,492 AP5Z1, FOXK1, 2 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 AP5Z1, RNU6-438P, 2682 more genes
    nsv3920006copy number variation1nstd102humanPathogenic GRCh37 chr7: 45,130-5,920,006 , GRCh38 chr7: 45,130-5,880,375 , NCBI36 chr7: 140,213-5,886,532 AP5Z1, RNU6-215P, 120 more genes
    nsv3894332copy number variation1nstd102humanPathogenic GRCh37 chr7: 1,201,674-5,175,651 , GRCh38.p12 chr7: 1,162,038-5,136,020 AP5Z1, FOXK1, 70 more genes
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