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Items: 1 to 20 of 124

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075539inversion1nstd229human GRCh38 chr19: 48,377,786-50,073,353 , GRCh37.p13 chr19: 48,881,043-50,576,610 SNRNP70, PTOV1, 126 more genes
    nsv7075255inversion1nstd229human GRCh38 chr19: 49,270,356-54,089,823 , GRCh37.p13 chr19: 49,773,613-54,528,887 FPR2, SNAR-A11, 344 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
    nsv7064925inversion1nstd229human GRCh38 chr19: 49,540,460-54,108,860 , GRCh37.p13 chr19: 50,043,717-54,528,887 DPRX, EMC10, 323 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
    nsv7014171copy number variation1nstd229human GRCh38 chr19: 49,647,170-49,647,356 , GRCh37.p13 chr19: 50,150,427-50,150,613 SCAF1
    nsv7008164copy number variation1nstd229human GRCh38 chr19: 49,656,160-49,656,403 , GRCh37.p13 chr19: 50,159,417-50,159,660 SCAF1
    nsv7004109copy number variation1nstd229human GRCh38 chr19: 49,651,401-49,651,771 , GRCh37.p13 chr19: 50,154,658-50,155,028 SCAF1
    nsv7002752copy number variation1nstd229human GRCh38 chr19: 49,637,134-49,639,945 , GRCh37.p13 chr19: 50,140,391-50,143,202 RRAS, SCAF1
    nsv6595834inversion1nstd223human GRCh38 chr19: 48,004,600-50,148,749 , GRCh37.p13 chr19: 48,507,857-50,652,006 KDELR1, VRK3, 155 more genes
    nsv6313906copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 49,911,081-53,127,438 , GRCh38.p12 chr19: 49,407,824-52,624,185 AP2A1, KLK3, 212 more genes
    nsv6310544copy number variation1nstd102humanUncertain significance GRCh37 chr19: 49,519,325-50,366,015 , GRCh38.p12 chr19: 49,016,068-49,862,758 CGB5, MED25, 76 more genes
    nsv6306758copy number variation1nstd186human GRCh37 chr19: 50,154,457-50,168,131 , GRCh38.p12 chr19: 49,651,200-49,664,874 IRF3, SCAF1, 1 more genes
    nsv6146786copy number variation1nstd206human GRCh38 chr19: 49,651,200-49,664,874 , GRCh37.p13 chr19: 50,154,457-50,168,131 IRF3, SCAF1, 1 more genes
    nsv6137808copy number variation1nstd102humanLikely pathogenic GRCh38.p12 chr19: 49,568,107-49,662,685 , GRCh37 chr19: 50,071,364-50,165,942 IRF3, PRRG2, 4 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
    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
    nsv5528568copy number variation1nstd206human GRCh38 chr19: 49,643,464-49,643,594 , GRCh37.p13 chr19: 50,146,721-50,146,851 SCAF1
    nsv5281351copy number variation1nstd204human GRCh38.p13 chr19: 49,645,539-49,648,011 , GRCh37.p13 chr19: 50,148,796-50,151,268 SCAF1
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