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Items: 1 to 20 of 1738

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112736copy number variation1nstd102humanPathogenic GRCh37 chr10: 48,301,535-51,807,296 , GRCh38.p12 chr10: 45,999,930-49,959,916 SHLD2P3, LOC100420617, 95 more genes
    nsv5916113copy number variation1nstd209human GRCh38 chr10: 45,791,488-50,132,032 , GRCh37.p13 chr10|NW_003871068.1: 62,603-2,281,126 , GRCh37.p13 chr10: 46,591,857-51,891,792 , LINC02675, 111 more genes
    nsv5914502copy number variation1nstd209human GRCh38 chr10: 45,768,833-50,109,449 , GRCh37.p13 chr10: 46,591,857-51,028,871 , GRCh37.p13 chr10|NW_003871068.1: 39,948-2,281,126 , AGAP13P, 111 more genes
    nsv5848672copy number variation2nstd209human GRCh38 chr10: 47,578,874-47,582,291 , GRCh37.p13 chr10|NW_003871068.1: 1,849,989-1,853,406 CTSLP2, ANXA8
    nsv5603501copy number variation1nstd207human GRCh38 chr10: 47,482,072-47,989,838 , GRCh37.p13 chr10: 47,746,310-48,254,623 , GRCh37.p13 chr10|NW_003871068.1: 1,753,187-2,179,734 , SYT15B, 16 more genes
    nsv5591057copy number variation1nstd207human GRCh38 chr10: 47,580,847-47,581,106 , GRCh37.p13 chr10|NW_003871068.1: 1,851,962-1,852,221 CTSLP2, ANXA8
    nsv5490696copy number variation1nstd206human GRCh38 chr10: 47,474,000-47,624,265 , GRCh37.p13 chr10|NW_003871068.1: 1,745,115-1,895,380 , DUSP8P1, 9 more genes
    nsv5380941copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 49,033,586-52,417,694 , GRCh38.p12 chr10: 45,999,930-49,959,916 CHAT, CTSLP2, 95 more genes
    nsv5259917copy number variation1nstd204human GRCh38.p13 chr10: 47,483,001-47,944,300 , GRCh37.p13 chr10|NW_003871068.1: 1,754,116-2,134,196 , SHLD2P3, 16 more genes
    nsv5259628copy number variation1nstd204human GRCh38.p13 chr10: 47,583,501-47,601,000 , GRCh37.p13 chr10|NW_003871068.1: 1,854,616-1,872,115 LINC02675, CTSLP2, 1 more genes
    nsv5257519copy number variation1nstd204human GRCh38.p13 chr10: 47,579,901-47,583,700 , GRCh37.p13 chr10|NW_003871068.1: 1,851,016-1,854,815 CTSLP2, ANXA8
    nsv5256747copy number variation1nstd204human GRCh38.p13 chr10: 47,578,401-47,585,000 , GRCh37.p13 chr10|NW_003871068.1: 1,849,516-1,856,115 CTSLP2, ANXA8
    nsv5250983copy number variation1nstd204human GRCh38.p13 chr10: 47,462,601-47,611,600 , GRCh37.p13 chr10|NW_003871068.1: 1,733,716-1,882,715 , GLUD1P6, 9 more genes
    nsv5246972copy number variation1nstd204human GRCh38.p13 chr10: 47,577,301-47,579,800 , GRCh37.p13 chr10|NW_003871068.1: 1,848,416-1,850,915 ANXA8, CTSLP2
    nsv5246600copy number variation1nstd204human GRCh38.p13 chr10: 47,583,401-47,591,700 , GRCh37.p13 chr10|NW_003871068.1: 1,854,516-1,862,815 LINC02675, ANXA8, 1 more genes
    nsv5246360copy number variation1nstd204human GRCh38.p13 chr10: 47,579,801-47,586,300 , GRCh37.p13 chr10|NW_003871068.1: 1,850,916-1,857,415 ANXA8, LINC02675, 1 more genes
    nsv5244625copy number variation1nstd204human GRCh38.p13 chr10: 47,579,801-47,611,600 , GRCh37.p13 chr10|NW_003871068.1: 1,850,916-1,882,715 LINC02675, ANXA8, 1 more genes
    nsv5243964copy number variation1nstd204human GRCh38.p13 chr10: 47,579,801-47,610,400 , GRCh37.p13 chr10|NW_003871068.1: 1,850,916-1,881,515 LINC02675, CTSLP2, 1 more genes
    nsv5243690copy number variation1nstd204human GRCh38.p13 chr10: 47,578,874-47,582,291 , GRCh37.p13 chr10|NW_003871068.1: 1,849,989-1,853,406 CTSLP2, ANXA8
    nsv5241878copy number variation1nstd204human GRCh38.p13 chr10: 47,579,301-47,582,400 , GRCh37.p13 chr10|NW_003871068.1: 1,850,416-1,853,515 ANXA8, CTSLP2
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