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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137724copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,785,250-23,491,592 , GRCh38.p12 chr1: 16,458,755-23,165,099 PADI1, RPS15AP6, 176 more genes
    nsv6137666copy number variation1nstd102humanPathogenic GRCh37 chrX: 91,829,757-113,050,225 , GRCh38.p12 chrX: 92,574,758-113,806,943 TCEAL8, MTND5P26, 272 more genes
    nsv6131637insertion1nstd186human GRCh37 chr16: 31,313,771-31,313,792 , GRCh38.p12 chr16: 31,302,450-31,302,471 ITGAM
    nsv6131459insertion1nstd186human GRCh37 chr22: 37,259,658-37,259,658 , GRCh38.p12 chr22: 36,863,616-36,863,616 , GRCh38.p12 chr22|NT_187631.1: 84,410-84,410 NCF4, NCF4-AS1
    nsv6131413insertion1nstd186human GRCh37 chr19: 46,022,710-46,023,020 , GRCh38.p12 chr19: 45,519,452-45,519,762 VASP, LOC107985315
    nsv6131202insertion1nstd186human GRCh37 chr19: 54,402,184-54,402,187 , GRCh38.p12 chr19: 53,898,930-53,898,933 PRKCG
    nsv6131079mobile element insertion1nstd186human GRCh37 chr17: 64,637,294-64,637,345 , GRCh38.p12 chr17: 66,641,176-66,641,227 PRKCA
    nsv6131054insertion1nstd186human GRCh37 chr16: 30,511,055-30,511,105 , GRCh38.p12 chr16: 30,499,734-30,499,784 ITGAL
    nsv6130884insertion1nstd186human GRCh37 chr21: 10,697,897-44,966,043 , GRCh38.p12 chr21: 12,965,809-43,546,162 , APP, 533 more genes
    nsv6129854insertion1nstd186human GRCh37 chr14: 69,417,180-69,417,230 , GRCh38.p12 chr14: 68,950,463-68,950,513 ACTN1
    nsv6129651insertion1nstd186human GRCh37 chr19: 6,816,558-6,816,598 , GRCh38.p12 chr19: 6,816,547-6,816,587 VAV1
    nsv6129564insertion1nstd186human GRCh37 chr16: 88,712,744-88,712,784 , GRCh38.p12 chr16: 88,646,336-88,646,376 CYBA
    nsv6128196insertion1nstd186human GRCh37 chr10: 68,181,607-68,181,655 , GRCh38.p12 chr10: 66,421,849-66,421,897 CTNNA3
    nsv6126556copy number variation1nstd186human GRCh37 chr17: 64,332,752-64,332,805 , GRCh38.p12 chr17: 66,336,634-66,336,687 PRKCA
    nsv6126127copy number variation1nstd186human GRCh37 chr21: 46,338,850-46,338,935 , GRCh38.p12 chr21: 44,918,935-44,919,020 ITGB2
    nsv6125861insertion1nstd186human GRCh37 chr6: 155,767,141-155,767,166 , GRCh38.p12 chr6: 155,446,007-155,446,032 NOX3
    nsv6125783copy number variation1nstd186human GRCh37 chr21: 37,864,449-37,864,758 , GRCh38.p12 chr21: 36,492,151-36,492,460 CLDN14, CLDN14-AS1
    nsv6124828insertion1nstd186human GRCh37 chr8: 141,960,170-141,960,193 , GRCh38.p12 chr8: 140,950,071-140,950,094 PTK2
    nsv6124744copy number variation1nstd186human GRCh37 chr18: 3,272,249-3,272,300 , GRCh38.p12 chr18: 3,272,251-3,272,302 MYL12B
    nsv6122886copy number variation1nstd186human GRCh37 chr16: 31,327,365-31,327,551 , GRCh38.p12 chr16: 31,316,044-31,316,230 ITGAM
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