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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    nsv7072237inversion1nstd229human GRCh38 chr19: 47,047,927-47,435,103 , GRCh37.p13 chr19: 47,551,185-47,938,360 MIR3190, C5AR1, 11 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
    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
    nsv7000997copy number variation1nstd229human GRCh38 chr19: 47,216,209-47,220,572 , GRCh37.p13 chr19: 47,719,466-47,723,829 BBC3
    nsv6598038inversion1nstd223human GRCh38 chr19: 45,719,988-49,018,154 , GRCh37.p13 chr19: 46,223,246-49,521,411 PLEKHA4, GAPDHP38, 150 more genes
    nsv6533545copy number variation1nstd223human GRCh38 chr19: 47,222,201-47,224,500 , GRCh37.p13 chr19: 47,725,458-47,727,757 BBC3
    nsv6525626copy number variation1nstd223human GRCh38 chr19: 47,216,239-47,219,265 , GRCh37.p13 chr19: 47,719,496-47,722,522 BBC3
    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
    nsv5980120insertion1nstd209human GRCh38 chr19: 47,226,081-47,226,081 , GRCh37.p13 chr19: 47,729,338-47,729,338 BBC3, MIR3191, 1 more genes
    nsv5937595copy number variation1nstd209human GRCh38 chr19: 47,233,231-47,233,839 , GRCh37.p13 chr19: 47,736,488-47,737,096 BBC3
    nsv5711346mobile element insertion1nstd211human GRCh38 chr19: 47,225,945-47,225,945 , GRCh37.p13 chr19: 47,729,202-47,729,202 BBC3, MIR3191, 1 more genes
    nsv5664469insertion1nstd207human GRCh38 chr19: 47,226,081-47,226,081 , GRCh37.p13 chr19: 47,729,338-47,729,338 BBC3, MIR3191, 1 more genes
    nsv5539433insertion1nstd206human GRCh38 chr19: 47,226,108-47,226,132 , GRCh37.p13 chr19: 47,729,365-47,729,389 BBC3, MIR3191, 1 more genes
    nsv5519886copy number variation1nstd206human GRCh38 chr19: 47,233,246-47,233,840 , GRCh37.p13 chr19: 47,736,503-47,737,097 BBC3
    nsv5327521copy number variation1nstd204human GRCh38.p13 chr19: 47,233,235-47,233,798 , GRCh37.p13 chr19: 47,736,492-47,737,055 BBC3
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