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Items: 1 to 20 of 141

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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
    nsv7058716inversion1nstd229human GRCh38 chr10: 72,663,272-73,189,528 , GRCh37.p13 chr10: 74,423,030-74,949,286 NUDT13, PLA2G12B, 10 more genes
    nsv6895110copy number variation1nstd229human GRCh38 chr10: 73,069,601-73,147,700 , GRCh37.p13 chr10: 74,829,359-74,907,458 P4HA1, ECD, 2 more genes
    nsv6893628copy number variation1nstd229human GRCh38 chr10: 72,714,112-73,254,102 , GRCh37.p13 chr10: 74,473,870-75,013,860 EIF4A2P2, MRPS16, 15 more genes
    nsv6887644copy number variation1nstd229human GRCh38 chr10: 73,129,713-73,140,268 , GRCh37.p13 chr10: 74,889,471-74,900,026 ECD, NUDT13
    nsv6881917copy number variation1nstd229human GRCh38 chr10: 73,084,901-73,215,400 , GRCh37.p13 chr10: 74,844,659-74,975,158 EIF4A2P2, LOC105378358, 5 more genes
    nsv6592173inversion1nstd223human GRCh38 chr10: 73,112,182-73,113,038 , GRCh37.p13 chr10: 74,871,940-74,872,796 NUDT13
    nsv6591529inversion1nstd223human GRCh38 chr10: 73,107,771-73,108,831 , GRCh37.p13 chr10: 74,867,529-74,868,589 NUDT13
    nsv6314185copy number variation1nstd102humanPathogenic GRCh37 chr10: 68,735,254-78,885,714 , GRCh38.p12 chr10: 66,975,496-77,125,956 SLC25A16, CTNNA3, 204 more genes
    nsv6314136copy number variation1nstd102humanUncertain significance GRCh37 chr10: 74,472,028-75,007,588 , GRCh38.p12 chr10: 72,712,270-73,247,830 MCU, DNAJC9, 14 more genes
    nsv6131974copy number variation1nstd213human GRCh37 chr10: 74,860,000-75,070,001 , GRCh38.p12 chr10: 73,100,242-73,310,243 MRPS16, LOC105378358, 9 more genes
    nsv6099786insertion1nstd212human GRCh38 chr10: 73,112,353-73,112,353 , GRCh37.p13 chr10: 74,872,111-74,872,111 NUDT13
    nsv5927101copy number variation1nstd209human GRCh38 chr10: 73,109,278-73,109,343 , GRCh37.p13 chr10: 74,869,036-74,869,101 NUDT13
    nsv5914351copy number variation1nstd209human GRCh38 chr10: 73,109,301-73,109,473 , GRCh37.p13 chr10: 74,869,059-74,869,231 NUDT13
    nsv5909992copy number variation1nstd209human GRCh38 chr10: 72,964,663-80,533,256 , GRCh37.p13 chr10: 74,724,421-82,293,012 , PRXL2A, 155 more genes
    nsv5696261mobile element insertion1nstd211human GRCh38 chr10: 73,128,404-73,128,404 , GRCh37.p13 chr10: 74,888,162-74,888,162 NUDT13
    nsv5550149insertion1nstd206human GRCh38 chr10: 73,112,366-73,112,404 , GRCh37.p13 chr10: 74,872,124-74,872,162 NUDT13
    nsv5399418mobile element insertion1nstd206human GRCh38 chr10: 73,128,404-73,128,455 , GRCh37.p13 chr10: 74,888,162-74,888,213 NUDT13
    nsv5126780mobile element insertion1nstd203human GRCh38 chr10: 73,112,353-73,112,366 , GRCh37.p13 chr10: 74,872,111-74,872,124 NUDT13
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