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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
    nsv7148114copy number variation1nstd102humanUncertain significance GRCh37 chr10: 112,021,329-113,054,313 , GRCh38.p12 chr10: 110,261,571-111,294,555 RBM20, MIR4680, 20 more genes
    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
    nsv7093858copy number variation1nstd102humanUncertain significance GRCh37 chr10: 111,860,412-112,839,579 , GRCh38.p12 chr10: 110,100,654-111,079,821 LOC105378479, LOC105378482, 22 more genes
    nsv7073198inversion1nstd229human GRCh38 chr10: 109,606,328-111,971,349 , GRCh37.p13 chr10: 111,366,086-113,731,107 LOC105378482, DUSP5, 33 more genes
    nsv7059252inversion1nstd229human GRCh38 chr10: 106,216,129-112,495,031 , GRCh37.p13 chr10: 107,975,887-114,254,790 LOC105378482, DUSP5, 64 more genes
    nsv6889711copy number variation1nstd229human GRCh38 chr10: 110,819,280-110,870,839 , GRCh37.p13 chr10: 112,579,038-112,630,597 PDCD4, RBM20, 1 more genes
    nsv6887507copy number variation1nstd229human GRCh38 chr10: 110,295,301-111,328,300 , GRCh37.p13 chr10: 112,055,059-113,088,058 HEAT2, BTBD7P2, 20 more genes
    nsv6885301copy number variation1nstd229human GRCh38 chr10: 110,780,328-116,002,717 , GRCh37.p13 chr10: 112,540,086-116,786,295 UBE2V1P5, MIR6715A, 66 more genes
    nsv6314085copy number variation1nstd102humanPathogenic GRCh37 chr10: 108,455,687-135,427,143 , GRCh38.p12 chr10: 106,695,929-133,613,639 LOC107984268, DPYSL4, 379 more genes
    nsv6309133copy number variation2nstd102humanUncertain significance GRCh37 chr10: 112,404,213-112,771,576 , GRCh38.p12 chr10: 110,644,455-111,011,818 RBM20, PDCD4, 8 more genes
    nsv6290874copy number variation1nstd102humanUncertain significance GRCh37 chr10: 107,092,654-117,852,548 , GRCh38.p12 chr10: 105,332,896-116,093,037 MIR6715B, SNRPGP12, 118 more genes
    nsv6131763copy number variation1nstd213human GRCh37 chr10: 110,950,000-112,790,001 , GRCh38.p12 chr10: 109,190,242-111,030,243 XPNPEP1, RNU4-5P, 30 more genes
    nsv5916653copy number variation1nstd209human GRCh38 chr10: 110,819,280-110,870,836 , GRCh37.p13 chr10: 112,579,038-112,630,594 PDCD4, RBM20, 1 more genes
    nsv4970642copy number variation1nstd200human GRCh38 chr10: 110,870,094-110,874,142 , GRCh37.p13 chr10: 112,629,852-112,633,900 PDCD4, PDCD4-AS1
    nsv4843405copy number variation1nstd200human GRCh37 chr10: 112,629,852-112,633,900 , GRCh38.p12 chr10: 110,870,094-110,874,142 PDCD4, PDCD4-AS1
    nsv4608598copy number variation1nstd183human GRCh37 chr10: 112,627,827-112,640,832 , GRCh38.p12 chr10: 110,868,069-110,881,074 PDCD4, PDCD4-AS1
    nsv4348764copy number variation1nstd102humanPathogenic GRCh37 chr10: 110,022,170-135,439,095 , GRCh38.p12 chr10: 108,262,412-133,625,591 LOC105378492, VENTX, 373 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
    nsv4177445copy number variation1nstd166human GRCh37.p13 chr10: 112,579,038-112,630,609 , GRCh38.p12 chr10: 110,819,280-110,870,851 RBM20, PDCD4, 1 more genes
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