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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076093inversion1nstd229human GRCh38 chr12: 108,420,843-108,466,871 , GRCh37.p13 chr12: 108,814,620-108,860,648 LINC01498
    nsv7075991inversion1nstd229human GRCh38 chr12: 108,471,685-108,485,926 , GRCh37.p13 chr12: 108,865,462-108,879,703 LINC01498
    nsv7061495inversion1nstd229human GRCh38 chr12: 107,014,490-109,497,170 , GRCh37.p13 chr12: 107,408,268-109,934,975 RPL17P38, RNU6-361P, 46 more genes
    nsv6937560copy number variation1nstd229human GRCh38 chr12: 107,811,784-108,715,214 , GRCh37.p13 chr12: 108,205,561-109,108,990 ISCU, LOC105369964, 16 more genes
    nsv6936301copy number variation1nstd229human GRCh38 chr12: 108,470,106-108,472,463 , GRCh37.p13 chr12: 108,863,883-108,866,240 LINC01498
    nsv6931501copy number variation1nstd229human GRCh38 chr12: 108,461,714-108,461,747 , GRCh37.p13 chr12: 108,855,491-108,855,524 LINC01498
    nsv6930841copy number variation1nstd229human GRCh38 chr12: 108,473,032-108,651,457 , GRCh37.p13 chr12: 108,866,809-109,045,233 SELPLG, SART3, 7 more genes
    nsv6929697copy number variation1nstd229human GRCh38 chr12: 108,136,392-108,487,917 , GRCh37.p13 chr12: 108,530,169-108,881,694 WSCD2, LOC196469, 3 more genes
    nsv6927082copy number variation1nstd229human GRCh38 chr12: 108,382,212-108,502,546 , GRCh37.p13 chr12: 108,775,989-108,896,323 LINC01498
    nsv6920046copy number variation1nstd229human GRCh38 chr12: 108,456,301-108,463,900 , GRCh37.p13 chr12: 108,850,078-108,857,677 LINC01498
    nsv6593542inversion1nstd223human GRCh38 chr12: 108,471,685-108,485,926 , GRCh37.p13 chr12: 108,865,462-108,879,703 LINC01498
    nsv6493274copy number variation1nstd223human GRCh38 chr12: 108,470,106-108,472,463 , GRCh37.p13 chr12: 108,863,883-108,866,240 LINC01498
    nsv6480495copy number variation1nstd223human GRCh38 chr12: 108,471,665-108,471,988 , GRCh37.p13 chr12: 108,865,442-108,865,765 LINC01498
    nsv6470333copy number variation1nstd223human GRCh38 chr12: 107,811,784-108,715,214 , GRCh37.p13 chr12: 108,205,561-109,108,990 LOC105369965, LINC01498, 16 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
    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
    nsv6081418insertion1nstd212human GRCh38 chr12: 108,470,526-108,470,526 , GRCh37.p13 chr12: 108,864,303-108,864,303 LINC01498
    nsv5932338copy number variation1nstd209human GRCh38 chr12: 108,470,106-108,472,462 , GRCh37.p13 chr12: 108,863,883-108,866,239 LINC01498
    nsv5854786copy number variation1nstd209human GRCh38 chr12: 108,470,128-108,472,427 , GRCh37.p13 chr12: 108,863,905-108,866,204 LINC01498
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