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Items: 1 to 20 of 181

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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
    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
    nsv6956657copy number variation1nstd229human GRCh38 chr13: 41,468,896-41,469,248 , GRCh37.p13 chr13: 42,043,032-42,043,384 RGCC
    nsv6951689copy number variation1nstd229human GRCh38 chr13: 41,470,973-41,481,931 , GRCh37.p13 chr13: 42,045,109-42,056,067 RGCC
    nsv6948330copy number variation1nstd229human GRCh38 chr13: 41,455,401-41,457,700 , GRCh37.p13 chr13: 42,029,537-42,031,836 RGCC
    nsv6947689copy number variation1nstd229human GRCh38 chr13: 41,267,754-41,560,314 , GRCh37.p13 chr13: 41,841,890-42,134,450 LOC105370174, OR7E37P, 10 more genes
    nsv6944762copy number variation1nstd229human GRCh38 chr13: 41,440,701-41,487,800 , GRCh37.p13 chr13: 42,014,837-42,061,936 OR7E155P, OR7E37P, 1 more genes
    nsv6638054copy number variation1nstd102humanUncertain significance GRCh37 chr13: 41,845,719-42,135,959 , GRCh38.p12 chr13: 41,271,583-41,561,823 OR7E37P, LOC105370174, 10 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
    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
    nsv6313982copy number variation1nstd102humanUncertain significance GRCh37 chr13: 39,428,367-43,608,103 , GRCh38.p12 chr13: 38,854,230-43,033,967 DGKH, ELF1, 82 more genes
    nsv6291787copy number variation1nstd102humanUncertain significance GRCh37 chr13: 41,845,718-42,124,117 , GRCh38.p12 chr13: 41,271,582-41,549,981 RNU6-57P, LOC105370174, 10 more genes
    nsv6289999copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 LINC00363, LOC105370118, 1334 more genes
    nsv6132644copy number variation1nstd213human GRCh37 chr13: 38,830,000-56,580,001 , GRCh38.p12 chr13: 38,255,863-56,005,867 , ATP7B, 305 more genes
    nsv6132543copy number variation1nstd213human GRCh37 chr13: 19,020,000-67,280,001 , GRCh38.p12 chr13: 18,445,862-66,705,869 , PARP4, 770 more genes
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