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Items: 1 to 20 of 174

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098899copy number variation1nstd102humanPathogenic GRCh37 chr13: 95,675,427-105,286,434 , GRCh38.p12 chr13: 95,023,173-104,634,083 PCCA, LOC105370340, 131 more genes
    nsv7077440inversion1nstd229human GRCh38 chr13: 95,324,680-102,597,006 , GRCh37.p13 chr13: 95,976,934-103,249,356 RN7SL60P, RPL15P18, 111 more genes
    nsv7072178inversion1nstd229human GRCh38 chr13: 97,997,035-104,548,310 , GRCh37.p13 chr13: 98,649,289-105,200,661 RNU1-24P, DOCK9, 95 more genes
    nsv6951775copy number variation1nstd229human GRCh38 chr13: 98,132,336-98,177,091 , GRCh37.p13 chr13: 98,784,590-98,829,345 LOC105370328, FARP1, 1 more genes
    nsv6951516copy number variation1nstd229human GRCh38 chr13: 97,991,801-98,907,000 , GRCh37.p13 chr13: 98,644,055-99,559,254 DOCK9, LOC107984566, 16 more genes
    nsv6950075copy number variation1nstd229human GRCh38 chr13: 97,917,201-98,288,900 , GRCh37.p13 chr13: 98,569,455-98,941,154 LOC107984566, LOC105370328, 6 more genes
    nsv6948757copy number variation1nstd229human GRCh38 chr13: 98,168,931-98,177,983 , GRCh37.p13 chr13: 98,821,185-98,830,237 FARP1, RNF113B
    nsv6946235copy number variation1nstd229human GRCh38 chr13: 98,169,792-98,212,396 , GRCh37.p13 chr13: 98,822,046-98,864,650 FARP1, RN7SKP8, 2 more genes
    nsv6942752copy number variation1nstd229human GRCh38 chr13: 97,718,301-98,378,600 , GRCh37.p13 chr13: 98,370,555-99,030,854 LOC105370327, FTLP8, 8 more genes
    nsv6638047copy number variation1nstd102humanPathogenic GRCh37 chr13: 75,268,539-115,107,733 , GRCh38.p12 chr13: 74,694,402-114,342,258 CUL4A, LOC105370373, 488 more genes
    nsv6637949copy number variation1nstd102humanUncertain significance GRCh37 chr13: 98,514,680-98,941,974 , GRCh38.p12 chr13: 97,862,426-98,289,720 MIR3170, RNF113B, 7 more genes
    nsv6637901copy number variation1nstd102humanUncertain significance GRCh37 chr13: 98,654,981-98,914,693 , GRCh38.p12 chr13: 98,002,727-98,262,439 LOC107984566, RN7SKP8, 5 more genes
    nsv6637727copy number variation1nstd102humanUncertain significance GRCh37 chr13: 98,720,234-99,172,213 , GRCh38.p12 chr13: 98,067,980-98,519,959 LOC105370328, LOC107984566, 6 more genes
    nsv6637615copy number variation1nstd102humanPathogenic GRCh37 chr13: 93,535,335-105,788,229 , GRCh38.p12 chr13: 92,883,082-105,135,878 SNORD13G, FTLP8, 162 more genes
    nsv6637400copy number variation1nstd102humanPathogenic GRCh37 chr13: 97,142,120-115,107,733 , GRCh38.p12 chr13: 96,489,866-114,342,258 LOC107984609, LINC00354, 265 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
    nsv6621986copy number variation1nstd224human GRCh37 chr13: 98,670,469-98,830,943 , GRCh38.p12 chr13: 98,018,215-98,178,689 LOC107984566, FARP1, 3 more genes
    nsv6495193copy number variation1nstd223human GRCh38 chr13: 98,132,331-98,177,135 , GRCh37.p13 chr13: 98,784,585-98,829,389 LOC105370328, FARP1, 1 more genes
    nsv6315552copy number variation1nstd102humanPathogenic GRCh37 chr13: 89,490,345-115,062,235 , GRCh38.p12 chr13: 88,838,091-114,296,760 MIR20A, MIR548AR, 347 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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