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Items: 1 to 20 of 122

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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
    nsv7072928inversion1nstd229human GRCh38 chr10: 110,494,552-110,498,214 , GRCh37.p13 chr10: 112,254,310-112,257,972 DUSP5-DT, DUSP5
    nsv7064221inversion1nstd229human GRCh38 chr10: 110,497,743-110,551,358 , GRCh37.p13 chr10: 112,257,501-112,311,116 DUSP5, RPL7P35
    nsv7059252inversion1nstd229human GRCh38 chr10: 106,216,129-112,495,031 , GRCh37.p13 chr10: 107,975,887-114,254,790 LOC105378482, DUSP5, 64 more genes
    nsv6895578copy number variation1nstd229human GRCh38 chr10: 110,506,623-110,506,811 , GRCh37.p13 chr10: 112,266,381-112,266,569 DUSP5
    nsv6893250copy number variation1nstd229human GRCh38 chr10: 110,495,307-110,496,108 , GRCh37.p13 chr10: 112,255,065-112,255,866 DUSP5, DUSP5-DT
    nsv6891065copy number variation1nstd229human GRCh38 chr10: 110,460,100-110,739,005 , GRCh37.p13 chr10: 112,219,858-112,498,763 RBM20, DUSP5-DT, 4 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
    nsv6620162copy number variation1nstd224human GRCh37 chr10: 112,082,992-112,316,956 , GRCh38.p12 chr10: 110,323,234-110,557,198 HMGB3P5, DUSP5, 3 more genes
    nsv6448621copy number variation1nstd223human GRCh38 chr10: 110,495,307-110,496,108 , GRCh37.p13 chr10: 112,255,065-112,255,866 DUSP5, DUSP5-DT
    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
    nsv6308977copy number variation1nstd102humanUncertain significance GRCh37 chr10: 111,860,412-112,404,423 , GRCh38.p12 chr10: 110,100,654-110,644,665 HMGB3P5, SMNDC1, 12 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
    nsv4837807copy number variation1nstd200human GRCh37 chr10: 112,269,938-112,269,990 , GRCh38.p12 chr10: 110,510,180-110,510,232 DUSP5
    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
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