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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5909873copy number variation1nstd209human GRCh38 chr10: 103,354,716-103,423,522 , GRCh37.p13 chr10: 105,114,473-105,183,279 TAF5, MIR1307, 2 more genes
    nsv5908075copy number variation1nstd209human GRCh38 chr10: 103,366,364-103,366,761 , GRCh37.p13 chr10: 105,126,121-105,126,518 TAF5
    nsv5860008copy number variation1nstd209human GRCh38 chr10: 103,355,875-103,367,091 , GRCh37.p13 chr10: 105,115,632-105,126,848 TAF5
    nsv5850763copy number variation1nstd209human GRCh38 chr10: 103,365,192-103,379,229 , GRCh37.p13 chr10: 105,124,949-105,138,986 TAF5
    nsv5317411copy number variation1nstd204human GRCh38.p13 chr10: 103,329,872-103,378,803 , GRCh37.p13 chr10: 105,089,629-105,138,560 TAF5, PCGF6
    nsv5308872copy number variation1nstd204human GRCh38.p13 chr10: 103,372,459-103,376,156 , GRCh37.p13 chr10: 105,132,216-105,135,913 TAF5
    nsv5252978copy number variation1nstd204human GRCh38.p13 chr10: 103,372,980-103,376,279 , GRCh37.p13 chr10: 105,132,737-105,136,036 TAF5
    nsv5242227copy number variation1nstd204human GRCh37.p13 chr10: 105,011,058-105,156,057 , GRCh38.p13 chr10: 103,251,301-103,396,300 TAF5, INA, 5 more genes
    nsv5131320mobile element insertion1nstd203human GRCh38 chr10: 103,367,834-103,367,847 , GRCh37.p13 chr10: 105,127,591-105,127,604 TAF5
    nsv4974002copy number variation1nstd200human GRCh38 chr10: 103,329,879-103,378,797 , GRCh37.p13 chr10: 105,089,636-105,138,554 PCGF6, TAF5
    nsv4970406copy number variation1nstd200human GRCh38 chr10: 103,372,467-103,376,149 , GRCh37.p13 chr10: 105,132,224-105,135,906 TAF5
    nsv4840859copy number variation1nstd200human GRCh37 chr10: 105,149,281-105,149,700 , GRCh38.p12 chr10: 103,389,524-103,389,943 ATP5MK, TAF5
    nsv4838998copy number variation1nstd200human GRCh37 chr10: 105,126,097-105,126,480 , GRCh38.p12 chr10: 103,366,340-103,366,723 TAF5
    nsv4832920copy number variation1nstd200human GRCh37 chr10: 105,089,636-105,138,554 , GRCh38.p12 chr10: 103,329,879-103,378,797 PCGF6, TAF5
    nsv4832227copy number variation1nstd200human GRCh37 chr10: 105,132,224-105,135,906 , GRCh38.p12 chr10: 103,372,467-103,376,149 TAF5
    nsv4729000copy number variation1nstd102humanUncertain significance GRCh37 chr10: 104,883,845-105,482,700 , GRCh38.p12 chr10: 103,124,088-103,722,942 INA, RNU11-3P, 16 more genes
    nsv4679283copy number variation1nstd189human GRCh37.p13 chr10: 104,468,424-105,156,097 , GRCh38.p12 chr10: 102,708,667-103,396,340 , ARL3, 25 more genes
    nsv4675057copy number variation1nstd102humanUncertain significance GRCh37 chr10: 104,915,576-105,241,844 , GRCh38.p12 chr10: 103,155,819-103,482,087 INA, NT5C2, 13 more genes
    nsv4488739mobile element insertion1nstd166human GRCh37.p13 chr10: 105,137,678-105,137,678 , GRCh38.p12 chr10: 103,377,921-103,377,921 TAF5
    nsv4457357copy number variation1nstd102humanUncertain significance GRCh37 chr10: 104,915,309-105,332,773 , GRCh38.p12 chr10: 103,155,552-103,573,016 PDCD11, TAF5, 14 more genes
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