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Items: 1 to 20 of 174

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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
    nsv7017689copy number variation1nstd229human GRCh38 chr19: 49,567,957-49,575,143 , GRCh37.p13 chr19: 50,071,214-50,078,400 NOSIP
    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
    nsv7001102copy number variation1nstd229human GRCh38 chr19: 49,576,280-49,577,653 , GRCh37.p13 chr19: 50,079,537-50,080,910 NOSIP
    nsv6598205inversion1nstd223human GRCh38 chr19: 49,563,604-49,564,218 , GRCh37.p13 chr19: 50,066,861-50,067,475 NOSIP
    nsv6598066inversion1nstd223human GRCh38 chr19: 49,571,907-49,572,408 , GRCh37.p13 chr19: 50,075,164-50,075,665 NOSIP
    nsv6597294inversion1nstd223human GRCh38 chr19: 49,565,669-49,566,177 , GRCh37.p13 chr19: 50,068,926-50,069,434 NOSIP
    nsv6597289inversion1nstd223human GRCh38 chr19: 49,553,080-49,554,555 , GRCh37.p13 chr19: 50,056,337-50,057,812 NOSIP
    nsv6596219inversion1nstd223human GRCh38 chr19: 49,553,403-49,554,419 , GRCh37.p13 chr19: 50,056,660-50,057,676 NOSIP
    nsv6595834inversion1nstd223human GRCh38 chr19: 48,004,600-50,148,749 , GRCh37.p13 chr19: 48,507,857-50,652,006 KDELR1, VRK3, 155 more genes
    nsv6525771copy number variation1nstd223human GRCh38 chr19: 49,551,035-49,554,494 , GRCh37.p13 chr19: 50,054,292-50,057,751 NOSIP
    nsv6523086copy number variation1nstd223human GRCh38 chr19: 49,549,921-49,554,313 , GRCh37.p13 chr19: 50,053,178-50,057,570 NOSIP
    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
    nsv6519202copy number variation1nstd223human GRCh38 chr19: 49,566,101-49,567,300 , GRCh37.p13 chr19: 50,069,358-50,070,557 NOSIP
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