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Items: 1 to 20 of 97

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142288insertion1nstd232human GRCh37.p13 chr19: 49,119,461-49,119,461 , GRCh38.p12 chr19: 48,616,204-48,616,204 RPL18
    nsv7095721copy number variation1nstd102humanUncertain significance GRCh37 chr19: 49,118,629-49,120,101 , GRCh38.p12 chr19: 48,615,372-48,616,844 FAM83E, RPL18
    nsv7075539inversion1nstd229human GRCh38 chr19: 48,377,786-50,073,353 , GRCh37.p13 chr19: 48,881,043-50,576,610 SNRNP70, PTOV1, 126 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
    nsv7064020inversion1nstd229human GRCh38 chr19: 48,004,601-50,148,757 , GRCh37.p13 chr19: 48,507,858-50,652,014 TEAD2, LHB, 155 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
    nsv7008233copy number variation1nstd229human GRCh38 chr19: 48,587,240-48,614,367 , GRCh37.p13 chr19: 49,090,497-49,117,624 FAM83E, RPL18, 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
    nsv6595834inversion1nstd223human GRCh38 chr19: 48,004,600-50,148,749 , GRCh37.p13 chr19: 48,507,857-50,652,006 KDELR1, VRK3, 155 more genes
    nsv6526815copy number variation1nstd223human GRCh38 chr19: 48,602,527-48,617,272 , GRCh37.p13 chr19: 49,105,784-49,120,529 RPL18, FAM83E, 1 more genes
    nsv6523344copy number variation1nstd223human GRCh38 chr19: 48,604,760-48,622,019 , GRCh37.p13 chr19: 49,108,017-49,125,276 SPACA4, RPL18, 2 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
    nsv6110571inversion1nstd212human GRCh38 chr19: 47,903,487-50,091,196 , GRCh37.p13 chr19: 48,406,744-50,594,453 , AP2A1, 155 more genes
    nsv5667352inversion1nstd207human GRCh38 chr19: 47,959,661-50,091,195 , GRCh37.p13 chr19: 48,462,918-50,594,452 , AP2A1, 145 more genes
    nsv5524652copy number variation1nstd206human GRCh38 chr19: 48,613,997-48,614,149 , GRCh37.p13 chr19: 49,117,254-49,117,406 FAM83E, RPL18
    nsv4730038copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 48,854,319-49,430,535 , GRCh38.p12 chr19: 48,351,062-48,927,278 BCAT2, CA11, 32 more genes
    nsv4729755copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886 SIGLEC5, MED25, 574 more genes
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