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Items: 1 to 20 of 199

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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
    nsv6957742copy number variation1nstd229human GRCh38 chr13: 41,524,610-41,969,915 , GRCh37.p13 chr13: 42,098,746-42,544,051 VWA8-AS1, RN7SL515P, 6 more genes
    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
    nsv6952424copy number variation1nstd229human GRCh38 chr13: 41,708,259-42,230,367 , GRCh37.p13 chr13: 42,282,395-42,804,503 RNU6-74P, KARS1P1, 8 more genes
    nsv6949692copy number variation1nstd229human GRCh38 chr13: 41,979,240-41,987,769 , GRCh37.p13 chr13: 42,553,376-42,561,905 LOC105370176, VWA8-AS1
    nsv6941760copy number variation1nstd229human GRCh38 chr13: 41,963,439-41,963,651 , GRCh37.p13 chr13: 42,537,575-42,537,787 VWA8-AS1
    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
    nsv6593490inversion1nstd223human GRCh38 chr13: 41,974,172-41,975,311 , GRCh37.p13 chr13: 42,548,308-42,549,447 VWA8-AS1, LOC105370176
    nsv6584656inversion1nstd223human GRCh38 chr13: 41,974,135-41,975,226 , GRCh37.p13 chr13: 42,548,271-42,549,362 LOC105370176, VWA8-AS1
    nsv6579377inversion1nstd223human GRCh38 chr13: 41,964,993-41,965,119 , GRCh37.p13 chr13: 42,539,129-42,539,255 VWA8-AS1
    nsv6484329copy number variation1nstd223human GRCh38 chr13: 41,950,510-41,959,743 , GRCh37.p13 chr13: 42,524,646-42,533,879 VWA8-AS1, VWA8
    nsv6483854copy number variation1nstd223human GRCh38 chr13: 41,524,610-41,969,916 , GRCh37.p13 chr13: 42,098,746-42,544,052 VWA8-AS1, VWA8, 6 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
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