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Items: 1 to 20 of 129

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148115copy number variation1nstd102humanUncertain significance GRCh37 chr15: 49,775,348-51,221,365 , GRCh38.p12 chr15: 49,483,151-50,929,168 RNA5SP395, AHCYP7, 24 more genes
    nsv7073737inversion1nstd229human GRCh38 chr15: 50,073,562-51,225,515 , GRCh37.p13 chr15: 50,365,759-51,517,712 DCAF13P3, TRPM7, 21 more genes
    nsv7067502inversion1nstd229human GRCh38 chr15: 48,513,881-51,354,383 , GRCh37.p13 chr15: 48,806,078-51,646,580 NDUFAF4P1, MIR4713, 49 more genes
    nsv6965201copy number variation1nstd229human GRCh38 chr15: 50,335,099-50,450,984 , GRCh37.p13 chr15: 50,627,296-50,743,181 AHCYP7, USP8, 5 more genes
    nsv6958676copy number variation1nstd229human GRCh38 chr15: 50,290,301-50,480,100 , GRCh37.p13 chr15: 50,582,498-50,772,297 USP8, MIR4712, 7 more genes
    nsv6637384copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,589,845-63,543,438 , GRCh38.p12 chr15: 48,297,648-63,251,239 LINC03065, FAM227B, 228 more genes
    nsv6595520inversion1nstd223human GRCh38 chr15: 50,073,559-51,225,509 , GRCh37.p13 chr15: 50,365,756-51,517,706 ATP8B4, TNFAIP8L3, 21 more genes
    nsv6586270inversion1nstd223human GRCh38 chr15: 50,348,437-50,348,658 , GRCh37.p13 chr15: 50,640,634-50,640,855 GABPB1, GABPB1-IT1
    nsv6513532copy number variation1nstd223human GRCh38 chr15: 50,349,001-50,351,000 , GRCh37.p13 chr15: 50,641,198-50,643,197 GABPB1, GABPB1-IT1
    nsv6315511copy number variation1nstd102humanUncertain significance GRCh37 chr15: 50,550,911-50,902,848 , GRCh38.p12 chr15: 50,258,714-50,610,651 USP8, USP50, 10 more genes
    nsv6313917copy number variation1nstd102humanPathogenic GRCh37 chr15: 47,635,238-56,509,908 , GRCh38.p12 chr15: 47,343,041-56,217,710 PYGO1, RNU6-449P, 125 more genes
    nsv6132897copy number variation1nstd213human GRCh37 chr15: 50,000,000-53,730,001 , GRCh38.p12 chr15: 49,707,803-53,437,804 MAPK6, ARPP19, 65 more genes
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5182560mobile element insertion1nstd203human GRCh38 chr15: 50,349,896-50,349,896 , GRCh37.p13 chr15: 50,642,093-50,642,093 GABPB1, GABPB1-IT1
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv5007521copy number variation1nstd200human GRCh38 chr15: 50,343,818-50,347,013 , GRCh37.p13 chr15: 50,636,015-50,639,210 RNU6-94P, GABPB1-IT1, 1 more genes
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4866113copy number variation1nstd200human GRCh37 chr15: 50,635,990-50,639,209 , GRCh38.p12 chr15: 50,343,793-50,347,012 RNU6-94P, GABPB1, 1 more genes
    nsv4769387copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,744,917-53,851,050 , GRCh38.p12 chr15: 48,452,720-53,558,853 BCL2L10, RNA5SP394, 86 more genes
    nsv4675095copy number variation1nstd102humanPathogenic GRCh37 chr15: 47,192,561-50,819,726 , GRCh38.p12 chr15: 46,900,363-50,527,529 LOC102724587, LOC645405, 51 more genes
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