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Items: 1 to 20 of 461

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7058460inversion1nstd229human GRCh38 chr19: 322,195-777,239 , GRCh37.p13 chr19: 322,195-777,239 PRSS57, RPS2P52, 23 more genes
    nsv7015012copy number variation1nstd229human GRCh38 chr19: 325,901-411,400 , GRCh37.p13 chr19: 325,901-411,400 MIER2, C2CD4C, 1 more genes
    nsv7008358copy number variation1nstd229human GRCh38 chr19: 376,752-507,545 , GRCh37.p13 chr19: 376,752-507,545 SHC2, RNA5SP462, 6 more genes
    nsv7006585copy number variation1nstd229human GRCh38 chr19: 387,915-576,682 , GRCh37.p13 chr19: 387,915-576,682 CDC34, C2CD4C, 9 more genes
    nsv7004680copy number variation1nstd229human GRCh38 chr19: 407,018-407,259 , GRCh37.p13 chr19: 407,018-407,259 C2CD4C
    nsv7003023copy number variation1nstd229human GRCh38 chr19: 402,534-416,297 , GRCh37.p13 chr19: 402,534-416,297 SHC2, C2CD4C
    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
    nsv6315518copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-2,256,387 , GRCh38.p12 chr19: 260,911-2,256,388 LOC100420586, RPS15, 113 more genes
    nsv6315510copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-1,319,319 , GRCh38.p12 chr19: 260,911-1,319,320 LOC101928450, LOC105372235, 66 more genes
    nsv6291797copy number variation1nstd102humanLikely benign GRCh37 chr19: 352,289-548,433 , GRCh38.p12 chr19: 352,289-548,433 TPGS1, GZMM, 8 more genes
    nsv6271689copy number variation1nstd214human GRCh38 chr19: 404,871-405,061 , GRCh37.p13 chr19: 404,871-405,061 C2CD4C
    nsv6133692copy number variation1nstd213human GRCh37 chr19: 180,000-2,200,001 , GRCh38.p12 chr19: 180,000-2,200,002 ATP5F1D, AZU1, 113 more genes
    nsv6112659insertion1nstd212human GRCh38 chr19: 404,996-404,996 , GRCh37.p13 chr19: 404,996-404,996 C2CD4C
    nsv6112035insertion1nstd212human GRCh38 chr19: 404,447-404,447 , GRCh37.p13 chr19: 404,447-404,447 C2CD4C
    nsv6111913insertion1nstd212human GRCh38 chr19: 404,810-404,810 , GRCh37.p13 chr19: 404,810-404,810 C2CD4C
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