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Items: 1 to 20 of 292

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130926insertion1nstd186human GRCh37 chr19: 50,520,186-50,520,212 , GRCh38.p12 chr19: 50,016,929-50,016,955 VRK3
    nsv6129420mobile element insertion1nstd186human GRCh37 chr19: 50,508,185-50,508,235 , GRCh38.p12 chr19: 50,004,928-50,004,978 VRK3
    nsv5974464inversion1nstd209human GRCh38 chr19: 49,769,209-52,432,690 , GRCh37.p13 chr19: 50,272,466-52,935,943 , AP2A1, 172 more genes
    nsv5969250inversion1nstd209human GRCh38 chr19: 49,972,119-49,985,651 , GRCh37.p13 chr19: 50,475,376-50,488,908 VRK3, SIGLEC16
    nsv5935916copy number variation1nstd209human GRCh38 chr19: 50,014,429-50,014,530 , GRCh37.p13 chr19: 50,517,686-50,517,787 VRK3
    nsv5886645copy number variation1nstd209human GRCh38 chr19: 50,004,778-50,006,116 , GRCh37.p13 chr19: 50,508,035-50,509,373 VRK3
    nsv5879756copy number variation1nstd209human GRCh38 chr19: 50,021,662-50,022,861 , GRCh37.p13 chr19: 50,524,919-50,526,118 VRK3
    nsv5718182mobile element insertion1nstd211human GRCh38 chr19: 50,004,928-50,004,928 , GRCh37.p13 chr19: 50,508,185-50,508,185 VRK3
    nsv5667352inversion1nstd207human GRCh38 chr19: 47,959,661-50,091,195 , GRCh37.p13 chr19: 48,462,918-50,594,452 , AP2A1, 145 more genes
    nsv5659450insertion1nstd207human GRCh38 chr19: 50,006,123-50,006,123 , GRCh37.p13 chr19: 50,509,380-50,509,380 VRK3
    nsv5593727copy number variation1nstd207human GRCh38 chr19: 50,004,930-50,006,115 , GRCh37.p13 chr19: 50,508,187-50,509,372 VRK3
    nsv5593647copy number variation1nstd207human GRCh38 chr19: 50,011,784-50,011,859 , GRCh37.p13 chr19: 50,515,041-50,515,116 VRK3
    nsv5560744mobile element insertion1nstd206human GRCh38 chr19: 50,004,928-50,004,978 , GRCh37.p13 chr19: 50,508,185-50,508,235 VRK3
    nsv5550066insertion1nstd206human GRCh38 chr19: 50,016,929-50,016,955 , GRCh37.p13 chr19: 50,520,186-50,520,212 VRK3
    nsv5530616copy number variation1nstd206human GRCh38 chr19: 50,014,429-50,014,536 , GRCh37.p13 chr19: 50,517,686-50,517,793 VRK3
    nsv5516385copy number variation1nstd206human GRCh38 chr19: 49,863,321-50,035,426 , GRCh37.p13 chr19: 50,366,578-50,538,683 IL4I1, SIGLEC11, 10 more genes
    nsv5297009copy number variation1nstd204human GRCh38.p13 chr19: 50,018,920-50,021,561 , GRCh37.p13 chr19: 50,522,177-50,524,818 VRK3
    nsv5285831copy number variation1nstd204human GRCh38.p13 chr19: 50,004,878-50,006,116 , GRCh37.p13 chr19: 50,508,135-50,509,373 VRK3
    nsv5282586copy number variation1nstd204human GRCh38.p13 chr19: 50,004,901-50,006,100 , GRCh37.p13 chr19: 50,508,158-50,509,357 VRK3
    nsv5206157mobile element deletion1nstd204human GRCh38.p13 chr19: 50,022,467-50,022,822 , GRCh37.p13 chr19: 50,525,724-50,526,079 VRK3
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