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Items: 1 to 20 of 187

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5705723mobile element insertion2nstd211human GRCh38 chr10: 49,989,643-49,989,643 , GRCh37.p13 chr10|NW_004504302.1: 168,818-168,818 , GRCh37.p13 chr10: 51,749,403-51,749,403 AGAP6, TIMM23B-AGAP6
    nsv5644124insertion1nstd207human GRCh38 chr10: 49,995,838-49,995,838 , GRCh37.p13 chr10: 51,755,598-51,755,598 , GRCh37.p13 chr10|NW_004504302.1: 175,013-175,013 AGAP6, TIMM23B-AGAP6
    nsv5544207insertion1nstd206human GRCh38 chr10: 49,987,284-49,987,290 , GRCh37.p13 chr10|NW_004504302.1: 166,459-166,465 , GRCh37.p13 chr10: 51,747,044-51,747,050 AGAP6, TIMM23B-AGAP6
    nsv5483515copy number variation1nstd206human GRCh38 chr10: 47,586,000-50,754,368 , GRCh37.p13 chr10: 46,591,857-52,514,128 HMGB1P50, PARG, 65 more genes
    nsv5479740copy number variation1nstd206human GRCh37.p13 chr10|NW_004504302.1: 53,543-193,543 , GRCh38 chr10: 49,874,368-50,014,368 PARG, AGAP6, 5 more genes
    nsv5478460copy number variation1nstd206human GRCh37.p13 chr10|NW_004504302.1: 177,409-250,675 , GRCh38 chr10: 49,998,234-50,071,500 , GRCh37.p13 chr10: 51,757,994-51,831,260 AGAP6, WASHC2A, 3 more genes
    nsv5257216copy number variation1nstd204human GRCh38.p13 chr10: 49,996,401-50,001,800 , GRCh37.p13 chr10: 51,756,161-51,761,560 , GRCh37.p13 chr10|NW_004504302.1: 175,576-180,975 TIMM23B-AGAP6, AGAP6
    nsv5255420copy number variation1nstd204human GRCh38.p13 chr10: 49,995,701-50,000,000 , GRCh37.p13 chr10|NW_004504302.1: 174,876-179,175 , GRCh37.p13 chr10: 51,755,461-51,759,760 AGAP6, TIMM23B-AGAP6
    nsv5254187copy number variation1nstd204human GRCh38.p13 chr10: 49,997,901-50,000,000 , GRCh37.p13 chr10: 51,757,661-51,759,760 , GRCh37.p13 chr10|NW_004504302.1: 177,076-179,175 AGAP6, TIMM23B-AGAP6
    nsv5242784copy number variation1nstd204human GRCh38.p13 chr10: 49,998,428-49,999,490 , GRCh37.p13 chr10|NW_004504302.1: 177,603-178,665 , GRCh37.p13 chr10: 51,758,188-51,759,250 AGAP6, TIMM23B-AGAP6
    nsv5137965mobile element insertion1nstd203human GRCh38 chr10: 49,989,627-49,989,643 , GRCh37.p13 chr10|NW_004504302.1: 168,802-168,818 , GRCh37.p13 chr10: 51,749,387-51,749,403 TIMM23B-AGAP6, AGAP6
    nsv5060032copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 46,966,535-51,874,356 , GRCh38.p12 chr10: 45,931,517-50,114,596 CHAT, CTSLP2, 104 more genes
    nsv5035636inversion1nstd200human GRCh38 chr10: 32,580,256-50,959,654 , GRCh37.p13 chr10: 32,869,184-52,719,414 , ZNF32-AS2, 320 more genes
    nsv5033632inversion1nstd200human GRCh38 chr10: 36,819,152-58,318,428 , GRCh37.p13 chr10: 37,108,080-60,078,188 , LOC107001062, 306 more genes
    nsv4969917copy number variation1nstd200human GRCh38 chr10: 50,005,345-50,011,010 , GRCh37.p13 chr10|NW_004504302.1: 184,520-190,185 , GRCh37.p13 chr10: 51,765,105-51,770,770 TIMM23B-AGAP6, AGAP6
    nsv4870857inversion1nstd200human GRCh37 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , NCOA4, 306 more genes
    nsv4729053copy number variation1nstd102humanLikely benign GRCh37 chr10: 51,753,154-52,166,339 , GRCh38.p12 chr10: 49,993,394-50,406,579 ASAH2, SLC9A3P3, 7 more genes
    nsv4716588copy number variation1nstd102humanPathogenic GRCh37 chr10: 46,964,973-51,826,226 , GRCh38.p12 chr10: 45,931,517-50,066,466 MAPK8, GDF10, 104 more genes
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