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Items: 1 to 20 of 150

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5828572copy number variation1nstd209human GRCh38 chr1: 183,614,636-183,619,597 , GRCh37.p13 chr1: 183,583,771-183,588,732 ARPC5
    nsv5441535copy number variation1nstd206human GRCh38 chr1: 183,613,517-183,619,258 , GRCh37.p13 chr1: 183,582,652-183,588,393 ARPC5
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5218087copy number variation1nstd204human GRCh38.p13 chr1: 183,614,661-183,619,597 , GRCh37.p13 chr1: 183,583,796-183,588,732 ARPC5
    nsv5200818copy number variation1nstd204human GRCh38.p13 chr1: 183,617,887-183,619,397 , GRCh37.p13 chr1: 183,587,022-183,588,532 ARPC5
    nsv4906654copy number variation1nstd200human GRCh38 chr1: 183,613,295-183,619,134 , GRCh37.p13 chr1: 183,582,430-183,588,269 ARPC5
    nsv4904094copy number variation1nstd200human GRCh38 chr1: 183,519,107-183,703,338 , GRCh37.p13 chr1: 183,488,242-183,672,473 , NCF2, 5 more genes
    nsv4784918copy number variation1nstd200human GRCh37 chr1: 183,582,459-183,588,275 , GRCh38.p12 chr1: 183,613,324-183,619,140 ARPC5
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4679470copy number variation1nstd189human GRCh37.p13 chr1: 183,284,304-183,608,085 , GRCh38.p12 chr1: 183,315,169-183,638,950 , NCF2, 7 more genes
    nsv4673925copy number variation1nstd102humanPathogenic GRCh37 chr1: 177,551,193-199,599,056 , GRCh38.p12 chr1: 177,582,058-199,629,928 QSOX1, PTPRC, 263 more genes
    nsv4459622mobile element insertion1nstd166human GRCh37.p13 chr1: 183,601,221-183,601,221 , GRCh38.p12 chr1: 183,632,086-183,632,086 ARPC5
    nsv4450583copy number variation1nstd102humanPathogenic GRCh37 chr1: 182,388,773-249,111,240 , GRCh38.p12 chr1: 182,419,638-248,817,041 RGS18, LINC02257, 1186 more genes
    nsv4399205copy number variation1nstd174human GRCh37 chr1: 183,581,363-183,589,167 , GRCh38.p12 chr1: 183,612,228-183,620,032 ARPC5
    nsv4380569copy number variation1nstd173human GRCh37 chr1: 183,521,307-183,594,102 , GRCh38.p12 chr1: 183,552,172-183,624,967 , ARPC5, 3 more genes
    nsv4327204inversion1nstd166human GRCh37.p13 chr1: 156,223,026-186,411,081 , GRCh38.p12 chr1: 156,253,235-186,441,949 , FASLG, 707 more genes
    nsv4072150copy number variation1nstd166human GRCh37.p13 chr1: 183,589,998-183,590,147 , GRCh38.p12 chr1: 183,620,863-183,621,012 ARPC5
    nsv3918947copy number variation1nstd102humanPathogenic NCBI36 chr1: 144,475,856-247,199,719 , GRCh37.p13 chr1: 145,764,499-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643 , LOC101060227, 1608 more genes
    nsv3912840copy number variation1nstd102humanPathogenic NCBI36 chr1: 144,764,751-247,199,719 , GRCh37.p13 chr1: 146,053,394-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643 , CRB1, 1608 more genes
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