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Items: 1 to 20 of 190

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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
    nsv5957999insertion1nstd209human GRCh38 chr10: 48,291,996-48,291,996 , GRCh37.p13 chr10: 49,500,039-49,500,039 RPS6P14
    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
    nsv5850307copy number variation1nstd209human GRCh38 chr10: 48,288,748-48,302,721 , GRCh37.p13 chr10: 49,496,791-49,510,764 RPS6P14
    nsv5641264insertion1nstd207human GRCh38 chr10: 48,291,994-48,291,994 , GRCh37.p13 chr10: 49,500,037-49,500,037 RPS6P14
    nsv5637321insertion1nstd207human GRCh38 chr10: 48,291,971-48,291,971 , GRCh37.p13 chr10: 49,500,014-49,500,014 RPS6P14
    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
    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
    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
    nsv4870857inversion1nstd200human GRCh37 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , NCOA4, 306 more genes
    nsv4769372copy number variation1nstd102humanUncertain significance GRCh37 chr10: 49,391,938-51,053,159 , GRCh38.p12 chr10: 48,183,895-49,845,113 HSPD1P17, FAM170B-AS1, 27 more genes
    nsv4761755insertion1nstd199human GRCh37 chr10: 49,500,024-49,500,024 , GRCh38.p12 chr10: 48,291,981-48,291,981 RPS6P14
    nsv4736384copy number variation1nstd199human GRCh37 chr10: 47,654,517-51,488,026 , GRCh38.p12 chr10: 45,931,517-49,929,364 , ARHGAP22-IT1, 99 more genes
    nsv4729305copy number variation1nstd102humanUncertain significance GRCh37 chr10: 48,750,425-51,386,904 , GRCh38.p12 chr10: 45,931,517-49,929,364 BMS1P7, NPY4R, 96 more genes
    nsv4728928copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 49,378,356-51,134,640 , GRCh38.p12 chr10: 48,170,313-49,926,594 CHAT, ERCC6, 28 more genes
    nsv4728845copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 47,132,305-51,627,470 , GRCh38.p12 chr10: 45,931,517-49,929,364 CHAT, CTSLP2, 96 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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