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Items: 1 to 20 of 134

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148237copy number variation1nstd102humanUncertain significance GRCh38 chr19: 47,257,435-47,886,413 , GRCh37.p13 chr19: 47,760,692-48,389,670 KPTN, RPL23AP80, 22 more genes
    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
    nsv7059316inversion1nstd229human GRCh38 chr19: 43,396,877-48,200,638 , GRCh37.p13 chr19: 43,901,029-48,703,895 GEMIN7, ZNF229, 212 more genes
    nsv7012960copy number variation1nstd229human GRCh38 chr19: 47,783,474-47,785,242 , GRCh37.p13 chr19: 48,286,731-48,288,499 SELENOW
    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
    nsv7006290copy number variation1nstd229human GRCh38 chr19: 47,781,388-47,784,287 , GRCh37.p13 chr19: 48,284,645-48,287,544 SELENOW
    nsv6625027copy number variation1nstd224human GRCh37 chr19: 48,254,792-48,305,340 , GRCh38.p12 chr19: 47,751,535-47,802,083 SELENOW, NOP53, 4 more genes
    nsv6625026copy number variation1nstd224human GRCh37 chr19: 48,201,967-48,368,777 , GRCh38.p12 chr19: 47,698,710-47,865,520 EHD2, LINC01595, 9 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
    nsv6531661copy number variation1nstd223human GRCh38 chr19: 47,771,888-47,812,888 , GRCh37.p13 chr19: 48,275,145-48,316,145 RPL23AP80, SELENOW, 1 more genes
    nsv6146370copy number variation1nstd206human GRCh38 chr19: 47,744,874-47,957,000 , GRCh37.p13 chr19: 48,248,131-48,460,257 SNAR-A12, SELENOW, 18 more genes
    nsv6133704copy number variation1nstd213human GRCh37 chr19: 45,030,000-55,230,001 , GRCh38.p12 chr19: 44,525,967-54,071,460 AP2A1, APOC1, 582 more genes
    nsv6133703copy number variation1nstd213human GRCh37 chr19: 41,220,000-49,640,001 , GRCh38.p12 chr19: 40,714,095-49,136,744 , APOC1, 402 more genes
    nsv6133474copy number variation1nstd213human GRCh37 chr19: 42,350,000-49,650,001 , GRCh38.p12 chr19: 41,845,937-49,146,744 , APOC1, 343 more genes
    nsv6107933insertion1nstd212human GRCh38 chr19: 47,783,905-47,783,905 , GRCh37.p13 chr19: 48,287,162-48,287,162 SELENOW
    nsv5558800sequence alteration1nstd206human GRCh38 chr19: 47,770,668-47,777,294 , GRCh37.p13 chr19: 48,273,925-48,280,551 SELENOW
    nsv5515671copy number variation1nstd206human GRCh38 chr19: 47,771,888-47,812,938 , GRCh37.p13 chr19: 48,275,145-48,316,195 TPRX1, RPL23AP80, 1 more genes
    nsv5288647copy number variation1nstd204human GRCh38.p13 chr19: 47,782,441-47,836,747 , GRCh37.p13 chr19: 48,285,698-48,340,004 TPRX1, SELENOW, 2 more genes
    nsv5284126copy number variation1nstd204human GRCh38.p13 chr19: 47,780,491-47,783,190 , GRCh37.p13 chr19: 48,283,748-48,286,447 SELENOW
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