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Items: 1 to 20 of 282

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073451inversion1nstd229human GRCh38 chr13: 39,843,646-49,674,098 , GRCh37.p13 chr13: 40,417,783-50,248,234 CYCSP34, FNDC3A, 195 more genes
    nsv6957992copy number variation1nstd229human GRCh38 chr13: 46,843,471-46,848,150 , GRCh37.p13 chr13: 47,417,606-47,422,285 HTR2A
    nsv6957544copy number variation1nstd229human GRCh38 chr13: 46,866,785-46,872,909 , GRCh37.p13 chr13: 47,440,920-47,447,044 HTR2A
    nsv6955552copy number variation1nstd229human GRCh38 chr13: 46,885,544-46,890,542 , GRCh37.p13 chr13: 47,459,679-47,464,677 HTR2A
    nsv6953024copy number variation1nstd229human GRCh38 chr13: 46,876,577-46,889,151 , GRCh37.p13 chr13: 47,450,712-47,463,286 HTR2A
    nsv6952483copy number variation1nstd229human GRCh38 chr13: 41,848,658-47,157,739 , GRCh37.p13 chr13: 42,422,794-47,731,874 TSC22D1-AS1, LINC00330, 105 more genes
    nsv6951969copy number variation1nstd229human GRCh38 chr13: 45,143,357-52,624,108 , GRCh37.p13 chr13: 45,717,492-53,198,243 SNRPGP14, EBPL, 158 more genes
    nsv6945228copy number variation1nstd229human GRCh38 chr13: 46,896,323-47,049,845 , GRCh37.p13 chr13: 47,470,458-47,623,980 HTR2A
    nsv6943934copy number variation1nstd229human GRCh38 chr13: 46,853,581-46,857,396 , GRCh37.p13 chr13: 47,427,716-47,431,531 HTR2A, HTR2A-AS1
    nsv6942761copy number variation1nstd229human GRCh38 chr13: 46,840,443-46,840,549 , GRCh37.p13 chr13: 47,414,578-47,414,684 HTR2A
    nsv6940692copy number variation1nstd229human GRCh38 chr13: 46,876,576-46,883,394 , GRCh37.p13 chr13: 47,450,711-47,457,529 HTR2A
    nsv6938765copy number variation1nstd229human GRCh38 chr13: 46,563,331-47,747,867 , GRCh37.p13 chr13: 47,137,466-48,322,002 LRCH1, ESD, 7 more genes
    nsv6938418copy number variation1nstd229human GRCh38 chr13: 46,883,461-46,889,150 , GRCh37.p13 chr13: 47,457,596-47,463,285 HTR2A
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6492307copy number variation1nstd223human GRCh38 chr13: 46,859,469-46,860,263 , GRCh37.p13 chr13: 47,433,604-47,434,398 HTR2A
    nsv6490358copy number variation1nstd223human GRCh38 chr13: 46,884,301-46,885,400 , GRCh37.p13 chr13: 47,458,436-47,459,535 HTR2A
    nsv6485820copy number variation1nstd223human GRCh38 chr13: 46,886,916-46,888,656 , GRCh37.p13 chr13: 47,461,051-47,462,791 HTR2A
    nsv6483808copy number variation1nstd223human GRCh38 chr13: 46,837,803-46,838,367 , GRCh37.p13 chr13: 47,411,938-47,412,502 HTR2A
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 more genes
    nsv6314198copy number variation1nstd102humanPathogenic GRCh37 chr13: 44,573,371-53,324,137 , GRCh38.p12 chr13: 43,999,235-52,750,002 PCNPP5, NRAD1, 189 more genes
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