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Items: 1 to 20 of 557

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146761copy number variation1nstd232human GRCh37.p13 chr19: 365,561-365,701 , GRCh38.p12 chr19: 365,561-365,701 SPMAP2
    nsv7140261copy number variation1nstd232human GRCh37.p13 chr19: 365,491-365,544 , GRCh38.p12 chr19: 365,491-365,544 SPMAP2
    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
    nsv7012064copy number variation1nstd229human GRCh38 chr19: 365,693-377,455 , GRCh37.p13 chr19: 365,693-377,455 SPMAP2
    nsv7008358copy number variation1nstd229human GRCh38 chr19: 376,752-507,545 , GRCh37.p13 chr19: 376,752-507,545 SHC2, RNA5SP462, 6 more genes
    nsv7007019copy number variation1nstd229human GRCh38 chr19: 326,264-402,755 , GRCh37.p13 chr19: 326,264-402,755 SPMAP2, MIER2
    nsv7004856copy number variation1nstd229human GRCh38 chr19: 371,601-380,300 , GRCh37.p13 chr19: 371,601-380,300 SPMAP2
    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
    nsv6534360copy number variation1nstd223human GRCh38 chr19: 360,195-506,451 , GRCh37.p13 chr19: 360,195-506,451 C2CD4C, CIMAP1D, 6 more genes
    nsv6532663copy number variation1nstd223human GRCh38 chr19: 360,101-361,100 , GRCh37.p13 chr19: 360,101-361,100 SPMAP2
    nsv6531209copy number variation1nstd223human GRCh38 chr19: 330,506-385,819 , GRCh37.p13 chr19: 330,506-385,819 SPMAP2, MIER2
    nsv6518286copy number variation1nstd223human GRCh38 chr19: 360,120-360,888 , GRCh37.p13 chr19: 360,120-360,888 SPMAP2
    nsv6517569copy number variation1nstd223human GRCh38 chr19: 364,107-396,593 , GRCh37.p13 chr19: 364,107-396,593 SPMAP2
    nsv6516526copy number variation1nstd223human GRCh38 chr19: 317,332-364,166 , GRCh37.p13 chr19: 317,332-364,166 MIER2, SPMAP2
    nsv6516266copy number variation1nstd223human GRCh38 chr19: 361,566-365,813 , GRCh37.p13 chr19: 361,566-365,813 SPMAP2
    nsv6315518copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-2,256,387 , GRCh38.p12 chr19: 260,911-2,256,388 LOC100420586, RPS15, 113 more genes
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