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Items: 1 to 20 of 190

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5956637insertion1nstd209human GRCh38 chr10: 93,693,673-93,693,673 , GRCh37.p13 chr10: 95,453,430-95,453,430 FRA10AC1
    nsv5924122copy number variation1nstd209human GRCh38 chr10: 93,699,022-93,699,086 , GRCh37.p13 chr10: 95,458,779-95,458,843 FRA10AC1
    nsv5921993copy number variation1nstd209human GRCh38 chr10: 90,979,234-99,692,336 , GRCh37.p13 chr10: 92,738,991-101,452,093 , CYP2C115P, 166 more genes
    nsv5710662mobile element insertion1nstd211human GRCh38 chr10: 93,670,882-93,670,882 , GRCh37.p13 chr10: 95,430,639-95,430,639 FRA10AC1
    nsv5703834mobile element insertion1nstd211human GRCh38 chr10: 93,667,212-93,667,212 , GRCh37.p13 chr10: 95,426,969-95,426,969 FRA10AC1
    nsv5640308insertion1nstd207human GRCh38 chr10: 93,702,522-93,702,522 , GRCh37.p13 chr10: 95,462,279-95,462,279 FRA10AC1
    nsv5625407insertion1nstd207human GRCh38 chr10: 93,702,516-93,702,516 , GRCh37.p13 chr10: 95,462,273-95,462,273 FRA10AC1
    nsv5412762mobile element insertion1nstd206human GRCh38 chr10: 93,667,212-93,667,263 , GRCh37.p13 chr10: 95,426,969-95,427,020 FRA10AC1
    nsv5406078mobile element insertion1nstd206human GRCh38 chr10: 93,670,882-93,670,933 , GRCh37.p13 chr10: 95,430,639-95,430,690 FRA10AC1
    nsv5365042translocation1nstd200human GRCh38 chr10: 93,702,534-93,702,534 , GRCh38 chr10: 93,702,245-93,702,245 , GRCh37.p13 chr10: 95,462,002-95,462,002 , GRCh37.p13 chr10: 95,462,291-95,462,291 FRA10AC1
    nsv5365041translocation1nstd200human GRCh38 chr10: 93,702,518-93,702,518 , GRCh38 chr10: 93,700,258-93,700,258 , GRCh37.p13 chr10: 95,460,015-95,460,015 , GRCh37.p13 chr10: 95,462,275-95,462,275 FRA10AC1
    nsv5347998translocation1nstd200human GRCh38 chr10: 93,701,888-93,701,888 , GRCh38 chr10: 93,702,535-93,702,535 , GRCh37.p13 chr10: 95,461,645-95,461,645 , GRCh37.p13 chr10: 95,462,292-95,462,292 FRA10AC1
    nsv5257659copy number variation1nstd204human GRCh38.p13 chr10: 93,685,401-93,688,200 , GRCh37.p13 chr10: 95,445,158-95,447,957 FRA10AC1
    nsv5137012mobile element insertion1nstd203human GRCh38 chr10: 93,670,874-93,670,882 , GRCh37.p13 chr10: 95,430,631-95,430,639 FRA10AC1
    nsv5127042mobile element insertion1nstd203human GRCh38 chr10: 93,667,199-93,667,212 , GRCh37.p13 chr10: 95,426,956-95,426,969 FRA10AC1
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4986722copy number variation1nstd200human GRCh38 chr10: 93,701,702-93,703,422 , GRCh37.p13 chr10: 95,461,459-95,463,179 FRA10AC1
    nsv4986721copy number variation1nstd200human GRCh38 chr10: 93,700,453-93,703,715 , GRCh37.p13 chr10: 95,460,210-95,463,472 FRA10AC1
    nsv4986720copy number variation1nstd200human GRCh38 chr10: 93,700,059-93,706,088 , GRCh37.p13 chr10: 95,459,816-95,465,845 FRA10AC1
    nsv4986719copy number variation1nstd200human GRCh38 chr10: 93,699,022-93,699,093 , GRCh37.p13 chr10: 95,458,779-95,458,850 FRA10AC1
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