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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
    nsv7065499inversion1nstd229human GRCh38 chr10: 35,933,937-37,620,453 , GRCh37.p13 chr10: 36,222,865-37,909,381 MTND1P18, LINC00993, 19 more genes
    nsv6893253copy number variation1nstd229human GRCh38 chr10: 37,334,801-37,351,700 , GRCh37.p13 chr10: 37,623,729-37,640,628 TMEM161BP1, LINC00993, 1 more genes
    nsv6883989copy number variation1nstd229human GRCh38 chr10: 36,906,541-37,474,418 , GRCh37.p13 chr10: 37,195,469-37,763,346 LOC105376497, LOC107984223, 11 more genes
    nsv6444065copy number variation1nstd223human GRCh38 chr10: 37,334,829-37,351,639 , GRCh37.p13 chr10: 37,623,757-37,640,567 TMEM161BP1, LINC00993, 1 more genes
    nsv6438673copy number variation1nstd223human GRCh38 chr10: 37,221,379-37,385,776 , GRCh37.p13 chr10: 37,510,307-37,674,704 ANKRD30A, TMEM161BP1, 5 more genes
    nsv6290893copy number variation1nstd102humannot provided GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579 C1QL3, LOC105376441, 774 more genes
    nsv6131955copy number variation1nstd213human GRCh37 chr10: 35,740,000-38,240,001 , GRCh38.p12 chr10: 35,451,072-37,951,073 CCNY, RPL7P37, 35 more genes
    nsv6131871copy number variation1nstd213human GRCh37 chr10: 37,360,000-37,990,001 , GRCh38.p12 chr10: 37,071,072-37,701,073 TMEM161BP1, MTND1P18, 13 more genes
    nsv5924459copy number variation1nstd209human GRCh38 chr10: 35,955,633-37,397,649 , GRCh37.p13 chr10: 36,244,561-37,686,577 , MKNK2P1, 15 more genes
    nsv5488790copy number variation1nstd206human GRCh38 chr10: 36,639,130-37,728,964 , GRCh37.p13 chr10: 36,928,058-38,017,892 , LOC105376496, 17 more genes
    nsv5123582mobile element insertion1nstd203human GRCh38 chr10: 37,335,742-37,335,771 , GRCh37.p13 chr10: 37,624,670-37,624,699 TMEM161BP1, LINC00993
    nsv5122441mobile element insertion1nstd203human GRCh38 chr10: 37,335,725-37,335,771 , GRCh37.p13 chr10: 37,624,653-37,624,699 TMEM161BP1, LINC00993
    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
    nsv4986242copy number variation1nstd200human GRCh38 chr10: 37,334,830-37,351,639 , GRCh37.p13 chr10: 37,623,758-37,640,567 VN1R53P, TMEM161BP1, 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
    nsv4675921copy number variation1nstd102humanLikely benign GRCh37 chr10: 37,189,335-38,900,673 , GRCh38.p12 chr10: 36,900,407-38,607,542 ZNF248, RNU6-1118P, 38 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
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