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Items: 1 to 20 of 471

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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
    nsv7058460inversion1nstd229human GRCh38 chr19: 322,195-777,239 , GRCh37.p13 chr19: 322,195-777,239 PRSS57, RPS2P52, 23 more genes
    nsv7006585copy number variation1nstd229human GRCh38 chr19: 387,915-576,682 , GRCh37.p13 chr19: 387,915-576,682 CDC34, C2CD4C, 9 more genes
    nsv7003740copy number variation1nstd229human GRCh38 chr19: 535,511-535,591 , GRCh37.p13 chr19: 535,511-535,591 CDC34
    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
    nsv6529938copy number variation1nstd223human GRCh38 chr19: 537,409-539,872 , GRCh37.p13 chr19: 537,409-539,872 CDC34
    nsv6522041copy number variation1nstd223human GRCh38 chr19: 498,192-592,352 , GRCh37.p13 chr19: 498,192-592,352 CDC34, HCN2, 7 more genes
    nsv6518623copy number variation1nstd223human GRCh38 chr19: 537,630-545,900 , GRCh37.p13 chr19: 537,630-545,900 CDC34, GZMM
    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
    nsv6307244copy number variation1nstd186human GRCh37 chr19: 540,269-540,649 , GRCh38.p12 chr19: 540,269-540,649 CDC34
    nsv6291797copy number variation1nstd102humanLikely benign GRCh37 chr19: 352,289-548,433 , GRCh38.p12 chr19: 352,289-548,433 TPGS1, GZMM, 8 more genes
    nsv6286552insertion1nstd214human GRCh38 chr19: 534,411-534,411 , GRCh37.p13 chr19: 534,411-534,411 CDC34
    nsv6278524copy number variation1nstd214human GRCh38 chr19: 534,622-534,797 , GRCh37.p13 chr19: 534,622-534,797 CDC34
    nsv6277479copy number variation1nstd214human GRCh38 chr19: 540,694-540,804 , GRCh37.p13 chr19: 540,694-540,804 CDC34
    nsv6204586copy number variation1nstd214human GRCh38 chr19: 534,636-534,856 , GRCh37.p13 chr19: 534,636-534,856 CDC34
    nsv6201478copy number variation1nstd214human GRCh38 chr19: 534,390-534,523 , GRCh37.p13 chr19: 534,390-534,523 CDC34
    nsv6195743copy number variation1nstd214human GRCh38 chr19: 539,958-540,070 , GRCh37.p13 chr19: 539,958-540,070 CDC34
    nsv6193059copy number variation1nstd214human GRCh38 chr19: 538,092-538,159 , GRCh37.p13 chr19: 538,092-538,159 CDC34
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