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Items: 1 to 20 of 207

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094477copy number variation1nstd102humanUncertain significance GRCh37 chr13: 41,367,363-43,181,054 , GRCh38.p12 chr13: 40,793,227-42,606,918 CYCSP34, RN7SL597P, 42 more genes
    nsv7075189inversion1nstd229human GRCh38 chr13: 38,938,572-45,892,931 , GRCh37.p13 chr13: 39,512,709-46,467,066 TPT1-AS1, AKAP11, 136 more genes
    nsv7075009inversion1nstd229human GRCh38 chr13: 42,255,185-44,636,659 , GRCh37.p13 chr13: 42,829,321-45,210,795 SERP2, DNAJC15, 35 more genes
    nsv7073451inversion1nstd229human GRCh38 chr13: 39,843,646-49,674,098 , GRCh37.p13 chr13: 40,417,783-50,248,234 CYCSP34, FNDC3A, 195 more genes
    nsv7063213inversion1nstd229human GRCh38 chr13: 39,276,739-42,681,969 , GRCh37.p13 chr13: 39,850,876-43,256,105 TPTE2P5, KBTBD7, 63 more genes
    nsv7060789inversion1nstd229human GRCh38 chr13: 38,967,784-43,058,064 , GRCh37.p13 chr13: 39,541,921-43,632,200 RGCC, RAC1P3, 79 more genes
    nsv6957461copy number variation1nstd229human GRCh38 chr13: 42,155,232-43,166,161 , GRCh37.p13 chr13: 42,729,368-43,740,297 TNFSF11, LINC00400, 15 more genes
    nsv6956383copy number variation1nstd229human GRCh38 chr13: 42,596,869-42,612,687 , GRCh37.p13 chr13: 43,171,005-43,186,823 TNFSF11
    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
    nsv6951279copy number variation1nstd229human GRCh38 chr13: 42,581,501-42,584,100 , GRCh37.p13 chr13: 43,155,637-43,158,236 TNFSF11
    nsv6947180copy number variation1nstd229human GRCh38 chr13: 42,551,824-42,561,700 , GRCh37.p13 chr13: 43,125,960-43,135,836 TNFSF11
    nsv6946837copy number variation1nstd229human GRCh38 chr13: 42,542,201-42,650,600 , GRCh37.p13 chr13: 43,116,337-43,224,736 TNFSF11
    nsv6946143copy number variation1nstd229human GRCh38 chr13: 42,588,265-43,144,864 , GRCh37.p13 chr13: 43,162,401-43,719,000 EPSTI1, LINC00400, 9 more genes
    nsv6938677copy number variation1nstd229human GRCh38 chr13: 42,559,891-42,562,386 , GRCh37.p13 chr13: 43,134,027-43,136,522 TNFSF11
    nsv6637284copy number variation1nstd102humanUncertain significance GRCh37 chr13: 43,163,676-43,717,925 , GRCh38.p12 chr13: 42,589,540-43,143,789 LOC105370179, LOC107984611, 9 more genes
    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
    nsv6481180copy number variation1nstd223human GRCh38 chr13: 42,554,701-42,579,500 , GRCh37.p13 chr13: 43,128,837-43,153,636 TNFSF11
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 more genes
    nsv6314117copy number variation1nstd102humanPathogenic GRCh37 chr13: 36,376,204-80,681,753 , GRCh38.p12 chr13: 35,802,067-80,107,618 RBM26, RNY4P31, 591 more genes
    nsv6314030copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,286-114,981,726 , GRCh38.p12 chr13: 18,862,146-114,216,251 RPSAP53, LOC105370213, 1310 more genes
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