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Items: 1 to 20 of 696

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148164copy number variation1nstd102humanPathogenic GRCh38 chr13: 106,425,676-114,326,445 , GRCh37.p13 chr13: 107,078,024-115,085,141 TUBGCP3, LINC01043, 132 more genes
    nsv7144797copy number variation1nstd232human GRCh37.p13 chr13: 114,185,992-114,186,046 , GRCh38.p12 chr13: 113,531,677-113,531,731 TMCO3
    nsv7137487copy number variation1nstd232human GRCh37.p13 chr13: 114,160,473-114,160,603 , GRCh38.p12 chr13: 113,506,158-113,506,288 TMCO3
    nsv7074580inversion1nstd229human GRCh38 chr13: 110,243,158-113,630,621 , GRCh37.p13 chr13: 110,895,505-114,284,936 LINC01070, NAXD, 71 more genes
    nsv7066153inversion1nstd229human GRCh38 chr13: 113,377,803-114,332,425 , GRCh37.p13 chr13: 114,032,118-115,085,141 TMCO3, GRK1, 26 more genes
    nsv7061212inversion1nstd229human GRCh38 chr13: 113,493,054-113,496,357 , GRCh37.p13 chr13: 114,147,369-114,150,672 TMCO3
    nsv6957419copy number variation1nstd229human GRCh38 chr13: 113,458,368-113,543,204 , GRCh37.p13 chr13: 114,112,683-114,197,519 TMCO3, RNU1-16P, 1 more genes
    nsv6955843copy number variation1nstd229human GRCh38 chr13: 113,528,721-113,528,756 , GRCh37.p13 chr13: 114,183,036-114,183,071 TMCO3
    nsv6953592copy number variation1nstd229human GRCh38 chr13: 113,518,201-113,536,200 , GRCh37.p13 chr13: 114,172,516-114,190,515 TMCO3
    nsv6953459copy number variation1nstd229human GRCh38 chr13: 113,529,321-113,529,390 , GRCh37.p13 chr13: 114,183,636-114,183,705 TMCO3
    nsv6952106copy number variation1nstd229human GRCh38 chr13: 113,350,847-113,586,194 , GRCh37.p13 chr13: 114,005,162-114,240,509 GRTP1, TFDP1, 5 more genes
    nsv6951518copy number variation1nstd229human GRCh38 chr13: 113,509,201-113,560,200 , GRCh37.p13 chr13: 114,163,516-114,214,515 TMCO3
    nsv6951501copy number variation1nstd229human GRCh38 chr13: 113,484,386-113,489,516 , GRCh37.p13 chr13: 114,138,701-114,143,831 DCUN1D2, TMCO3
    nsv6948846copy number variation1nstd229human GRCh38 chr13: 113,491,716-113,497,232 , GRCh37.p13 chr13: 114,146,031-114,151,547 TMCO3, DCUN1D2
    nsv6947349copy number variation1nstd229human GRCh38 chr13: 113,550,201-113,554,100 , GRCh37.p13 chr13: 114,204,516-114,208,415 TMCO3
    nsv6946968copy number variation1nstd229human GRCh38 chr13: 113,503,630-113,552,739 , GRCh37.p13 chr13: 114,157,945-114,207,054 TMCO3
    nsv6945684copy number variation1nstd229human GRCh38 chr13: 113,486,201-113,490,800 , GRCh37.p13 chr13: 114,140,516-114,145,115 TMCO3, DCUN1D2
    nsv6944035copy number variation1nstd229human GRCh38 chr13: 113,541,222-113,541,507 , GRCh37.p13 chr13: 114,195,537-114,195,822 TMCO3
    nsv6943198copy number variation1nstd229human GRCh38 chr13: 111,028,013-113,621,089 , GRCh37.p13 chr13: 111,680,360-114,275,404 ARHGEF7, GRTP1, 52 more genes
    nsv6942847copy number variation1nstd229human GRCh38 chr13: 113,098,406-113,791,902 , GRCh37.p13 chr13: 113,752,720-114,494,875 MIR8075, ATP4B, 22 more genes
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