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Items: 1 to 20 of 162

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139021insertion1nstd232human GRCh37.p13 chr19: 47,342,843-47,342,843 , GRCh38.p12 chr19: 46,839,586-46,839,586 AP2S1
    nsv7137151copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 47,028,919-48,185,409 , GRCh38.p12 chr19: 46,525,662-47,682,152 C5AR1, CALM3, 36 more genes
    nsv7074444inversion1nstd229human GRCh38 chr19: 46,843,865-46,849,221 , GRCh37.p13 chr19: 47,347,122-47,352,478 AP2S1
    nsv7074377inversion1nstd229human GRCh38 chr19: 41,965,396-49,981,454 , GRCh37.p13 chr19: 42,514,712-50,484,711 IGFL1, SYMPK, 400 more genes
    nsv7073220inversion1nstd229human GRCh38 chr19: 45,719,988-49,018,157 , GRCh37.p13 chr19: 46,223,246-49,521,414 RUVBL2, NTN5, 150 more genes
    nsv7066709inversion1nstd229human GRCh38 chr19: 40,109,835-46,893,669 , GRCh37.p13 chr19: 40,615,742-47,396,926 LOC105372405, RNU6-611P, 305 more genes
    nsv7062827inversion1nstd229human GRCh38 chr19: 46,836,371-46,876,727 , GRCh37.p13 chr19: 47,339,628-47,379,984 ARHGAP35, AP2S1
    nsv7059316inversion1nstd229human GRCh38 chr19: 43,396,877-48,200,638 , GRCh37.p13 chr19: 43,901,029-48,703,895 GEMIN7, ZNF229, 212 more genes
    nsv7013389copy number variation1nstd229human GRCh38 chr19: 46,780,374-46,918,351 , GRCh37.p13 chr19: 47,283,631-47,421,608 ARHGAP35, SLC1A5, 3 more genes
    nsv7012452copy number variation1nstd229human GRCh38 chr19: 45,998,776-48,954,957 , GRCh37.p13 chr19: 46,502,034-49,458,214 TMEM160, SNORD23, 131 more genes
    nsv7012144copy number variation1nstd229human GRCh38 chr19: 46,835,431-46,837,258 , GRCh37.p13 chr19: 47,338,688-47,340,515 AP2S1
    nsv7002702copy number variation1nstd229human GRCh38 chr19: 46,839,304-46,839,333 , GRCh37.p13 chr19: 47,342,561-47,342,590 AP2S1
    nsv6625023copy number variation1nstd224human GRCh37 chr19: 47,276,054-47,346,158 , GRCh38.p12 chr19: 46,772,797-46,842,901 SLC1A5, HNRNPMP2, 2 more genes
    nsv6598038inversion1nstd223human GRCh38 chr19: 45,719,988-49,018,154 , GRCh37.p13 chr19: 46,223,246-49,521,411 PLEKHA4, GAPDHP38, 150 more genes
    nsv6597905inversion1nstd223human GRCh38 chr19: 46,836,655-46,837,150 , GRCh37.p13 chr19: 47,339,912-47,340,407 AP2S1
    nsv6534372copy number variation1nstd223human GRCh38 chr19: 46,835,431-46,837,258 , GRCh37.p13 chr19: 47,338,688-47,340,515 AP2S1
    nsv6525846copy number variation1nstd223human GRCh38 chr19: 46,782,084-46,917,902 , GRCh37.p13 chr19: 47,285,341-47,421,159 HNRNPMP2, ARHGAP35, 3 more genes
    nsv6522179copy number variation1nstd223human GRCh38 chr19: 46,843,259-46,914,923 , GRCh37.p13 chr19: 47,346,516-47,418,180 AP2S1, ARHGAP35
    nsv6516104copy number variation1nstd223human GRCh38 chr19: 46,832,955-46,836,357 , GRCh37.p13 chr19: 47,336,212-47,339,614 AP2S1
    nsv6310692copy number variation1nstd102humanUncertain significance GRCh37 chr19: 47,341,704-47,354,023 , GRCh38.p12 chr19: 46,838,447-46,850,766 AP2S1
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