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Items: 1 to 20 of 288

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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
    nsv6956546copy number variation1nstd229human GRCh38 chr13: 41,553,233-41,553,353 , GRCh37.p13 chr13: 42,127,369-42,127,489 LOC105370174
    nsv6955245copy number variation1nstd229human GRCh38 chr13: 41,563,461-41,568,124 , GRCh37.p13 chr13: 42,137,597-42,142,260 VWA8, MIR5006, 1 more genes
    nsv6954723copy number variation1nstd229human GRCh38 chr13: 41,556,181-41,556,642 , GRCh37.p13 chr13: 42,130,317-42,130,778 LOC105370174
    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
    nsv6944184copy number variation1nstd229human GRCh38 chr13: 41,529,768-41,531,772 , GRCh37.p13 chr13: 42,103,904-42,105,908 LOC105370174
    nsv6941429copy number variation1nstd229human GRCh38 chr13: 41,550,814-41,564,110 , GRCh37.p13 chr13: 42,124,950-42,138,246 LOC105370175, LOC105370174
    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
    nsv6584127inversion1nstd223human GRCh38 chr13: 41,561,864-41,562,289 , GRCh37.p13 chr13: 42,136,000-42,136,425 LOC105370174
    nsv6491822copy number variation1nstd223human GRCh38 chr13: 41,529,768-41,531,768 , GRCh37.p13 chr13: 42,103,904-42,105,904 LOC105370174
    nsv6486819copy number variation1nstd223human GRCh38 chr13: 41,563,461-41,568,123 , GRCh37.p13 chr13: 42,137,597-42,142,259 MIR5006, LOC105370174, 1 more genes
    nsv6486070copy number variation1nstd223human GRCh38 chr13: 41,510,191-41,515,239 , GRCh37.p13 chr13: 42,084,327-42,089,375 LOC105370174
    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
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