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Items: 1 to 20 of 150

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974464inversion1nstd209human GRCh38 chr19: 49,769,209-52,432,690 , GRCh37.p13 chr19: 50,272,466-52,935,943 , AP2A1, 172 more genes
    nsv5667352inversion1nstd207human GRCh38 chr19: 47,959,661-50,091,195 , GRCh37.p13 chr19: 48,462,918-50,594,452 , AP2A1, 145 more genes
    nsv5516385copy number variation1nstd206human GRCh38 chr19: 49,863,321-50,035,426 , GRCh37.p13 chr19: 50,366,578-50,538,683 IL4I1, SIGLEC11, 10 more genes
    nsv5024817copy number variation1nstd200human GRCh38 chr19: 49,856,044-49,921,115 , GRCh37.p13 chr19: 50,359,301-50,424,372 IL4I1, AKT1S1, 6 more genes
    nsv5021013copy number variation1nstd200human GRCh38 chr19: 49,904,979-49,906,475 , GRCh37.p13 chr19: 50,408,236-50,409,732 IL4I1, NUP62
    nsv4853351copy number variation1nstd200human GRCh37 chr19: 50,416,129-50,416,468 , GRCh38.p12 chr19: 49,912,872-49,913,211 NUP62, IL4I1
    nsv4853350copy number variation1nstd200human GRCh37 chr19: 50,408,255-50,409,704 , GRCh38.p12 chr19: 49,904,998-49,906,447 IL4I1, NUP62
    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
    nsv4685764copy number variation1nstd102humannot provided GRCh37 chr19: 47,939,842-54,626,871 , GRCh38.p12 chr19: 47,436,585-54,071,460 SNAR-G1, IRF3, 453 more genes
    nsv4676357copy number variation1nstd102humanPathogenic GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308 MIR4324, KLK9, 485 more genes
    nsv4627115copy number variation1nstd183human GRCh37 chr19: 50,427,995-50,504,630 , GRCh38.p12 chr19: 49,924,738-50,001,373 ATF5, NUP62, 5 more genes
    nsv4514090mobile element insertion1nstd166human GRCh37.p13 chr19: 50,425,638-50,425,638 , GRCh38.p12 chr19: 49,922,381-49,922,381 NUP62, IL4I1
    nsv4513382mobile element insertion1nstd166human GRCh37.p13 chr19: 50,414,630-50,414,630 , GRCh38.p12 chr19: 49,911,373-49,911,373 NUP62, IL4I1
    nsv4457465copy number variation1nstd102humanUncertain significance GRCh37 chr19: 49,600,909-51,366,070 , GRCh38.p12 chr19: 49,097,652-50,862,814 MED25, EMC10, 117 more genes
    nsv4415256copy number variation1nstd174human GRCh37 chr19: 50,422,019-50,504,411 , GRCh38.p12 chr19: 49,918,762-50,001,154 ATF5, NUP62, 5 more genes
    nsv4376838copy number variation1nstd173human GRCh37 chr19: 48,462,617-51,107,899 , GRCh38.p12 chr19: 47,959,360-50,604,642 , LIN7B, 173 more genes
    nsv4321864inversion1nstd166human GRCh37.p13 chr19: 46,657,897-51,634,775 , GRCh38.p12 chr19: 46,154,640-51,131,518 , C5AR1, 288 more genes
    nsv4269085copy number variation1nstd166human GRCh37.p13 chr19: 50,379,628-50,456,858 , GRCh38.p12 chr19: 49,876,371-49,953,601 ATF5, NUP62, 6 more genes
    nsv4265650copy number variation1nstd166human GRCh37.p13 chr19: 50,408,256-50,409,704 , GRCh38.p12 chr19: 49,904,999-49,906,447 IL4I1, NUP62
    nsv4263166copy number variation1nstd166human GRCh37.p13 chr19: 50,419,945-50,422,387 , GRCh38.p12 chr19: 49,916,688-49,919,130 IL4I1, NUP62
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