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Items: 1 to 20 of 919

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145096copy number variation1nstd232human GRCh37.p13 chr19: 443,977-444,036 , GRCh38.p12 chr19: 443,977-444,036 SHC2
    nsv7073159inversion1nstd229human GRCh38 chr19: 249,047-1,189,238 , GRCh37.p13 chr19: 249,047-1,189,237 MADCAM1-AS1, ARID3A, 53 more genes
    nsv7063137inversion1nstd229human GRCh38 chr19: 363,262-504,084 , GRCh37.p13 chr19: 363,262-504,084 SHC2, SPMAP2, 5 more genes
    nsv7059826inversion1nstd229human GRCh38 chr19: 412,742-415,933 , GRCh37.p13 chr19: 412,742-415,933 SHC2
    nsv7058460inversion1nstd229human GRCh38 chr19: 322,195-777,239 , GRCh37.p13 chr19: 322,195-777,239 PRSS57, RPS2P52, 23 more genes
    nsv7017858copy number variation1nstd229human GRCh38 chr19: 444,518-456,529 , GRCh37.p13 chr19: 444,518-456,529 RNA5SP462, SHC2
    nsv7014412copy number variation1nstd229human GRCh38 chr19: 416,301-418,900 , GRCh37.p13 chr19: 416,301-418,900 SHC2
    nsv7012729copy number variation1nstd229human GRCh38 chr19: 452,101-461,800 , GRCh37.p13 chr19: 452,101-461,800 CIMAP1D, SHC2, 1 more genes
    nsv7011561copy number variation1nstd229human GRCh38 chr19: 429,182-429,656 , GRCh37.p13 chr19: 429,182-429,656 SHC2
    nsv7011078copy number variation1nstd229human GRCh38 chr19: 461,253-476,228 , GRCh37.p13 chr19: 461,253-476,228 SHC2, CIMAP1D
    nsv7008358copy number variation1nstd229human GRCh38 chr19: 376,752-507,545 , GRCh37.p13 chr19: 376,752-507,545 SHC2, RNA5SP462, 6 more genes
    nsv7007955copy number variation1nstd229human GRCh38 chr19: 441,393-441,976 , GRCh37.p13 chr19: 441,393-441,976 SHC2
    nsv7006585copy number variation1nstd229human GRCh38 chr19: 387,915-576,682 , GRCh37.p13 chr19: 387,915-576,682 CDC34, C2CD4C, 9 more genes
    nsv7003023copy number variation1nstd229human GRCh38 chr19: 402,534-416,297 , GRCh37.p13 chr19: 402,534-416,297 SHC2, C2CD4C
    nsv7001880copy number variation1nstd229human GRCh38 chr19: 459,901-461,400 , GRCh37.p13 chr19: 459,901-461,400 SHC2, CIMAP1D
    nsv6637450copy number variation1nstd102humanUncertain significance GRCh37 chr19: 260,912-508,202 , GRCh38.p12 chr19: 260,912-508,202 VN2R11P, C2CD4C, 9 more genes
    nsv6637255copy number variation1nstd102humanUncertain significance GRCh37 chr19: 260,912-538,303 , GRCh38.p12 chr19: 260,912-538,303 C2CD4C, CDC34, 10 more genes
    nsv6624895copy number variation1nstd224human GRCh37 chr19: 388,413-606,473 , GRCh38.p12 chr19: 388,413-606,473 BSG-AS1, HCN2, 11 more genes
    nsv6534360copy number variation1nstd223human GRCh38 chr19: 360,195-506,451 , GRCh37.p13 chr19: 360,195-506,451 C2CD4C, CIMAP1D, 6 more genes
    nsv6533167copy number variation1nstd223human GRCh38 chr19: 410,958-417,094 , GRCh37.p13 chr19: 410,958-417,094 SHC2
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