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Items: 1 to 20 of 108

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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
    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
    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
    nsv5255021copy number variation1nstd204human GRCh38.p13 chr10: 49,938,419-49,981,097 , GRCh37.p13 chr10|NW_004504302.1: 117,594-160,272 PARG, TIMM23B, 3 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
    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
    nsv4679068copy number variation1nstd189human GRCh37.p13 chr10: 46,556,721-51,801,243 , GRCh38.p12 chr10: 45,931,517-50,041,483 , CHAT, 106 more genes
    nsv4678848copy number variation1nstd189human GRCh37.p13 chr10: 46,556,721-51,910,312 , GRCh38.p12 chr10: 45,931,517-50,150,552 , CHAT, 108 more genes
    nsv4675455copy number variation1nstd102humanPathogenic GRCh37 chr10: 50,250,603-69,256,083 , GRCh38.p12 chr10: 45,931,517-67,496,325 MRLN, LOC102724778, 242 more genes
    nsv4457096copy number variation1nstd102humanUncertain significance GRCh37 chr10: 49,378,356-52,467,181 , GRCh38.p12 chr10: 45,999,930-49,959,916 OGDHL, PTPN20, 95 more genes
    nsv4456956copy number variation1nstd102humanUncertain significance GRCh37 chr10: 46,966,533-51,850,064 , GRCh38.p12 chr10: 45,931,517-50,090,304 NPY4R, LOC105378577, 104 more genes
    nsv4455730copy number variation1nstd102humanUncertain significance GRCh37 chr10: 46,287,086-51,830,366 , GRCh38.p12 chr10: 45,791,638-50,070,606 LOC102724593, GPRIN2, 108 more genes
    nsv4455643copy number variation1nstd102humanUncertain significance GRCh37 chr10: 48,252,674-51,830,366 , GRCh38.p12 chr10: 45,999,930-49,959,916 OGDHL, SHLD2P1, 95 more genes
    nsv4455118copy number variation1nstd102humanPathogenic GRCh37 chr10: 46,235,357-51,874,163 , GRCh38.p12 chr10: 45,739,909-50,114,403 DUSP8P2, FAM170B, 108 more genes
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