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Items: 1 to 20 of 118

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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
    nsv7008893copy number variation1nstd229human GRCh38 chr19: 49,584,449-49,588,243 , GRCh37.p13 chr19: 50,087,706-50,091,500 PRRG2
    nsv7004882copy number variation1nstd229human GRCh38 chr19: 49,540,401-49,583,500 , GRCh37.p13 chr19: 50,043,658-50,086,757 PRRG2, RCN3, 1 more genes
    nsv7003792copy number variation1nstd229human GRCh38 chr19: 49,578,001-49,581,600 , GRCh37.p13 chr19: 50,081,258-50,084,857 PRRG2, NOSIP
    nsv6595834inversion1nstd223human GRCh38 chr19: 48,004,600-50,148,749 , GRCh37.p13 chr19: 48,507,857-50,652,006 KDELR1, VRK3, 155 more genes
    nsv6535322copy number variation1nstd223human GRCh38 chr19: 49,582,728-49,585,905 , GRCh37.p13 chr19: 50,085,985-50,089,162 PRRG2
    nsv6522188copy number variation1nstd223human GRCh38 chr19: 49,578,055-49,581,589 , GRCh37.p13 chr19: 50,081,312-50,084,846 NOSIP, PRRG2
    nsv6521022copy number variation1nstd223human GRCh38 chr19: 49,540,406-49,586,977 , GRCh37.p13 chr19: 50,043,663-50,090,234 RCN3, NOSIP, 1 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
    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
    nsv6133706copy number variation1nstd213human GRCh37 chr19: 49,520,000-50,090,001 , GRCh38.p12 chr19: 49,016,743-49,586,744 CD37, CGB3, 51 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
    nsv6042122copy number variation1nstd212human GRCh38 chr19: 49,578,839-49,578,905 , GRCh37.p13 chr19: 50,082,096-50,082,162 PRRG2, NOSIP
    nsv5667352inversion1nstd207human GRCh38 chr19: 47,959,661-50,091,195 , GRCh37.p13 chr19: 48,462,918-50,594,452 , AP2A1, 145 more genes
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