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Items: 1 to 20 of 74

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7093715copy number variation1nstd102humanUncertain significance GRCh37 chr10: 52,834,351-53,227,616 , GRCh38.p12 chr10: 51,074,591-51,467,856 MIR605, PRKG1, 1 more genes
    nsv7076978inversion1nstd229human GRCh38 chr10: 49,556,263-52,217,922 , GRCh37.p13 chr10: 50,764,309-53,977,682 A1CF, NPAP1P1, 36 more genes
    nsv7060309inversion1nstd229human GRCh38 chr10: 46,173,677-55,799,586 , GRCh37.p13 chr10: 46,591,857-57,559,346 NPY4R, LOC102724603, 138 more genes
    nsv6887274copy number variation1nstd229human GRCh38 chr10: 51,041,701-51,437,100 , GRCh37.p13 chr10: 52,801,461-53,196,860 PRKG1, MIR605, 2 more genes
    nsv6886834copy number variation1nstd229human GRCh38 chr10: 45,568,878-51,464,891 , GRCh37.p13 chr10: 46,064,326-53,224,651 PGBD3, MAPK8, 134 more genes
    nsv6886123copy number variation1nstd229human GRCh38 chr10: 51,044,145-51,404,106 , GRCh37.p13 chr10: 52,803,905-53,163,866 PRKG1, MIR605, 2 more genes
    nsv6453388copy number variation1nstd223human GRCh38 chr10: 51,269,223-51,326,789 , GRCh37.p13 chr10: 53,028,983-53,086,549 MIR605, PRKG1, 1 more genes
    nsv6444846copy number variation1nstd223human GRCh38 chr10: 51,044,145-51,404,106 , GRCh37.p13 chr10: 52,803,905-53,163,866 MIR605, PRKG1, 2 more genes
    nsv6442471copy number variation1nstd223human GRCh38 chr10: 51,295,801-51,297,700 , GRCh37.p13 chr10: 53,055,561-53,057,460 MIR605, PRKG1
    nsv6132043copy number variation1nstd213human GRCh37 chr10: 53,050,000-53,540,001 , GRCh38.p12 chr10: 51,290,240-51,780,241 PRKG1, CSTF2T, 2 more genes
    nsv5033632inversion1nstd200human GRCh38 chr10: 36,819,152-58,318,428 , GRCh37.p13 chr10: 37,108,080-60,078,188 , LOC107001062, 306 more genes
    nsv4973628copy number variation1nstd200human GRCh38 chr10: 51,044,145-51,404,109 , GRCh37.p13 chr10: 52,803,905-53,163,869 PRKG1, MIR605, 2 more genes
    nsv4969954copy number variation1nstd200human GRCh38 chr10: 51,269,223-51,326,789 , GRCh37.p13 chr10: 53,028,983-53,086,549 RSU1P3, PRKG1, 1 more genes
    nsv4870857inversion1nstd200human GRCh37 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , NCOA4, 306 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
    nsv4455880copy number variation1nstd102humanUncertain significance GRCh37 chr10: 52,082,714-53,320,354 , GRCh38.p12 chr10: 50,322,954-51,560,594 SGMS1, CTSLP4, 16 more genes
    nsv4389374copy number variation1nstd171human GRCh37 chr10: 53,057,466-53,057,500 , GRCh38.p12 chr10: 51,297,706-51,297,740 PRKG1, MIR605
    nsv4343722sequence alteration1nstd166human GRCh37.p13 chr10: 43,905,894-92,001,956 , GRCh38.p12 chr10: 43,410,446-90,242,199 , ALOX5, 749 more genes
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