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Items: 1 to 20 of 560

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146393copy number variation1nstd232human GRCh37.p13 chr10: 117,956,168-117,956,218 , GRCh38.p12 chr10: 116,196,656-116,196,706 GFRA1
    nsv7141933copy number variation1nstd232human GRCh37.p13 chr10: 117,956,140-117,956,218 , GRCh38.p12 chr10: 116,196,628-116,196,706 GFRA1
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7075724inversion1nstd229human GRCh38 chr10: 116,161,594-116,173,771 , GRCh37.p13 chr10: 117,921,106-117,933,283 GFRA1
    nsv7074631inversion1nstd229human GRCh38 chr10: 116,200,073-116,204,675 , GRCh37.p13 chr10: 117,959,585-117,964,187 GFRA1
    nsv7068515inversion1nstd229human GRCh38 chr10: 116,251,144-116,254,514 , GRCh37.p13 chr10: 118,010,656-118,014,026 GFRA1
    nsv7060011inversion1nstd229human GRCh38 chr10: 116,124,560-116,728,658 , GRCh37.p13 chr10: 117,884,071-118,348,516 PNLIPRP1, PNLIPP1, 13 more genes
    nsv7058604inversion1nstd229human GRCh38 chr10: 116,162,480-116,173,811 , GRCh37.p13 chr10: 117,921,992-117,933,323 GFRA1
    nsv6897787copy number variation1nstd229human GRCh38 chr10: 116,264,530-116,264,658 , GRCh37.p13 chr10: 118,024,042-118,024,170 GFRA1
    nsv6897669copy number variation1nstd229human GRCh38 chr10: 116,158,225-116,160,356 , GRCh37.p13 chr10: 117,917,737-117,919,868 GFRA1
    nsv6897482copy number variation1nstd229human GRCh38 chr10: 116,098,150-116,101,108 , GRCh37.p13 chr10: 117,857,661-117,860,619 GFRA1
    nsv6896616copy number variation1nstd229human GRCh38 chr10: 116,161,035-116,161,300 , GRCh37.p13 chr10: 117,920,547-117,920,812 GFRA1
    nsv6896374copy number variation1nstd229human GRCh38 chr10: 116,077,964-116,085,267 , GRCh37.p13 chr10: 117,837,475-117,844,778 GFRA1
    nsv6895405copy number variation1nstd229human GRCh38 chr10: 116,064,054-116,064,097 , GRCh37.p13 chr10: 117,823,565-117,823,608 GFRA1
    nsv6893248copy number variation1nstd229human GRCh38 chr10: 116,158,814-116,160,815 , GRCh37.p13 chr10: 117,918,326-117,920,327 GFRA1
    nsv6892707copy number variation1nstd229human GRCh38 chr10: 116,066,001-116,073,100 , GRCh37.p13 chr10: 117,825,512-117,832,611 GFRA1
    nsv6892692copy number variation1nstd229human GRCh38 chr10: 116,049,016-116,059,953 , GRCh37.p13 chr10: 117,808,527-117,819,464 GFRA1
    nsv6889697copy number variation1nstd229human GRCh38 chr10: 116,158,970-116,164,027 , GRCh37.p13 chr10: 117,918,482-117,923,539 GFRA1
    nsv6887499copy number variation1nstd229human GRCh38 chr10: 116,141,652-116,146,960 , GRCh37.p13 chr10: 117,901,163-117,906,471 GFRA1
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