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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094120copy number variation1nstd102humanUncertain significance GRCh37 chr12: 109,921,357-110,034,382 , GRCh38.p12 chr12: 109,483,552-109,596,577 MVK, RNU4-32P, 2 more genes
    nsv7069534inversion1nstd229human GRCh38 chr12: 109,510,753-109,510,877 , GRCh37.p13 chr12: 109,948,558-109,948,682 UBE3B
    nsv7061495inversion1nstd229human GRCh38 chr12: 107,014,490-109,497,170 , GRCh37.p13 chr12: 107,408,268-109,934,975 RPL17P38, RNU6-361P, 46 more genes
    nsv6931732copy number variation1nstd229human GRCh38 chr12: 108,914,683-113,697,537 , GRCh37.p13 chr12: 109,308,459-114,135,342 PTPN11, RPL31P49, 111 more genes
    nsv6922947copy number variation1nstd229human GRCh38 chr12: 108,490,015-109,627,369 , GRCh37.p13 chr12: 108,883,792-110,065,174 RNU4-32P, LOC105369968, 30 more genes
    nsv6920631copy number variation1nstd229human GRCh38 chr12: 109,500,443-109,500,710 , GRCh37.p13 chr12: 109,938,248-109,938,515 UBE3B
    nsv6621489copy number variation1nstd224human GRCh37 chr12: 109,201,326-110,355,704 , GRCh38.p12 chr12: 108,807,550-109,917,899 FAM222A, MYO1H, 29 more genes
    nsv6291583copy number variation1nstd102humanPathogenic GRCh37 chr12: 104,230,462-111,984,801 , GRCh38.p12 chr12: 103,836,684-111,546,997 LOC105369964, LOC644746, 147 more genes
    nsv6248577mobile element insertion1nstd215human GRCh38 chr12: 109,492,366-109,492,366 , GRCh37.p13 chr12: 109,930,171-109,930,171 UBE3B
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132406copy number variation1nstd213human GRCh37 chr12: 108,420,000-110,500,001 , GRCh38.p12 chr12: 108,026,223-110,062,196 DAO, SART3, 47 more genes
    nsv6122319copy number variation1nstd186human GRCh37 chr12: 109,930,171-109,930,284 , GRCh38.p12 chr12: 109,492,366-109,492,479 UBE3B
    nsv6088082insertion1nstd212human GRCh38 chr12: 109,526,507-109,526,507 , GRCh37.p13 chr12: 109,964,312-109,964,312 UBE3B
    nsv5976909insertion1nstd209human GRCh38 chr12: 109,492,356-109,492,356 , GRCh37.p13 chr12: 109,930,161-109,930,161 UBE3B
    nsv5864345copy number variation1nstd209human GRCh38 chr12: 109,512,903-109,516,305 , GRCh37.p13 chr12: 109,950,708-109,954,110 UBE3B
    nsv5710519mobile element insertion2nstd211human GRCh38 chr12: 109,492,366-109,492,366 , GRCh37.p13 chr12: 109,930,171-109,930,171 UBE3B
    nsv5658408insertion1nstd207human GRCh38 chr12: 109,492,356-109,492,356 , GRCh37.p13 chr12: 109,930,161-109,930,161 UBE3B
    nsv5497711copy number variation1nstd206human GRCh38 chr12: 109,492,366-109,492,479 , GRCh37.p13 chr12: 109,930,171-109,930,284 UBE3B
    nsv5365215translocation1nstd200human GRCh38 chr12: 109,519,786-109,519,786 , GRCh38 chr12: 109,519,861-109,519,861 , GRCh37.p13 chr12: 109,957,591-109,957,591 , GRCh37.p13 chr12: 109,957,666-109,957,666 UBE3B
    nsv5343890translocation1nstd200human GRCh37 chr12: 109,957,592-109,957,592 , GRCh37 chr12: 109,957,666-109,957,666 , GRCh38.p12 chr12: 109,519,787-109,519,787 , GRCh38.p12 chr12: 109,519,861-109,519,861 UBE3B
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