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Items: 1 to 20 of 1528

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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
    nsv5910146copy number variation1nstd209human GRCh38 chr10: 46,108,417-47,381,921 , GRCh37.p13 chr10|NW_003871068.1: 379,532-1,653,036 , SYT15, 35 more genes
    nsv5666496inversion1nstd207human GRCh38 chr10: 46,395,606-47,470,096 , GRCh37.p13 chr10|NW_003871068.1: 666,721-1,741,211 , GDF2, 29 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
    nsv5380788copy number variation1nstd102humanUncertain significance GRCh37 chr10: 48,383,844-48,386,037 , GRCh38.p12 chr10: 47,353,325-47,355,518 RBP3
    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
    nsv4969871copy number variation1nstd200human GRCh38 chr10: 47,346,932-47,347,527 , GRCh37.p13 chr10: 48,391,835-48,392,430 , GRCh37.p13 chr10|NW_003871068.1: 1,618,047-1,618,642 RBP3
    nsv4870857inversion1nstd200human GRCh37 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , NCOA4, 306 more genes
    nsv4761292inversion1nstd199human GRCh37 chr10: 46,688,427-47,529,172 , GRCh38.p12 chr10: 46,157,935-47,923,579 , CTSLP2, 54 more genes
    nsv4760577inversion1nstd199human GRCh37 chr10: 47,151,095-47,770,398 , GRCh38.p12 chr10: 46,157,935-47,739,149 , CTSLP2, 51 more genes
    nsv4756522inversion1nstd199human GRCh37 chr10: 47,151,095-48,278,724 , GRCh38.p12 chr10: 46,157,935-47,739,149 , CTSLP2, 51 more genes
    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
    nsv4730095inversion14nstd198human GRCh38 chr10: 46,314,931-48,071,682 , GRCh37.p13 chr10|NW_003871068.1: 586,046-2,261,578 , CTSLP2, 55 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
    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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