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Items: 1 to 20 of 83

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3910270copy number variation1nstd102humanPathogenic GRCh38 chr13: 18,445,862-114,327,173 , NCBI36 chr13: 10,098,739-114,110,750 , GRCh37 chr13: 19,020,001-115,085,141 SLC15A1, RNU6-71P, 1332 more genes
    nsv3924528copy number variation1nstd102humanPathogenic GRCh37 chr13: 41,516,434-115,085,141 , GRCh38 chr13: 40,942,298-114,340,331 , NCBI36 chr13: 40,414,434-114,123,908 SLC15A1, LOC105370271, 925 more genes
    nsv4675850copy number variation1nstd102humanPathogenic GRCh37 chr13: 53,262,013-115,107,733 , GRCh38.p12 chr13: 52,687,878-114,342,258 SLC15A1, TEX30, 680 more genes
    nsv3907697copy number variation1nstd102humanPathogenic GRCh37 chr13: 53,551,300-109,850,651 , GRCh38.p12 chr13: 52,977,165-109,198,303 SLC15A1, GPC5, 565 more genes
    nsv6314171copy number variation1nstd102humanPathogenic GRCh37 chr13: 79,370,012-115,107,733 , GRCh38.p12 chr13: 78,795,877-114,342,258 SLC15A1, MIR4705, 430 more genes
    nsv3901091copy number variation1nstd102humanPathogenic GRCh37 chr13: 80,572,498-108,719,528 , GRCh38.p12 chr13: 79,998,363-108,067,180 SLC15A1, KRT18P27, 295 more genes
    nsv3920102copy number variation1nstd102humanPathogenic GRCh38 chr13: 86,788,927-114,340,331 , GRCh37 chr13: 87,441,182-115,085,141 , NCBI36 chr13: 86,239,183-114,123,908 SLC15A1, LOC107984609, 369 more genes
    nsv3903376copy number variation1nstd102humanPathogenic GRCh37 chr13: 88,073,140-115,107,733 , GRCh38.p12 chr13: 87,420,885-114,342,258 SLC15A1, ZIC2, 364 more genes
    nsv3896487copy number variation1nstd102humanPathogenic GRCh37 chr13: 89,796,110-115,083,342 , GRCh38.p12 chr13: 89,143,856-114,317,867 SLC15A1, TMTC4, 347 more genes
    nsv3904416copy number variation1nstd102humanPathogenic GRCh37 chr13: 81,851,091-102,864,674 , GRCh38.p12 chr13: 81,276,956-102,212,324 SLC15A1, TRF-GAA1-5, 224 more genes
    nsv3890560copy number variation1nstd102humanPathogenic GRCh37 chr13: 94,474,530-115,107,733 , GRCh38.p12 chr13: 93,822,277-114,342,258 SLC15A1, RPL15P18, 303 more genes
    nsv3892450copy number variation1nstd102humanPathogenic GRCh37 chr13: 96,586,481-115,107,733 , GRCh38.p12 chr13: 95,934,227-114,342,258 SLC15A1, RPS6P23, 268 more genes
    nsv4675644copy number variation1nstd102humanPathogenic GRCh37 chr13: 96,895,656-115,107,733 , GRCh38.p12 chr13: 96,243,402-114,342,258 SLC15A1, ZIC2, 266 more genes
    nsv6637400copy number variation1nstd102humanPathogenic GRCh37 chr13: 97,142,120-115,107,733 , GRCh38.p12 chr13: 96,489,866-114,342,258 SLC15A1, LOC107984609, 265 more genes
    nsv5672796copy number variation1nstd102humanPathogenic GRCh37 chr13: 94,679,977-111,536,145 , GRCh38.p12 chr13: 94,027,723-110,883,798 SLC15A1, LINC00359, 220 more genes
    nsv3914527copy number variation1nstd102humanPathogenic GRCh38 chr13: 93,345,058-109,458,154 , NCBI36 chr13: 92,795,312-108,908,502 , GRCh37 chr13: 93,997,311-110,110,501 SLC15A1, DOCK9, 196 more genes
    nsv3904662copy number variation1nstd102humanPathogenic GRCh37 chr13: 94,703,767-109,731,879 , GRCh38.p12 chr13: 94,051,513-109,079,531 SLC15A1, LOC107984615, 189 more genes
    nsv7148239copy number variation1nstd102humanPathogenic GRCh38 chr13: 98,343,655-110,990,677 , GRCh37.p13 chr13: 98,995,909-111,643,024 SLC15A1, CLYBL-AS3, 162 more genes
    nsv6637615copy number variation1nstd102humanPathogenic GRCh37 chr13: 93,535,335-105,788,229 , GRCh38.p12 chr13: 92,883,082-105,135,878 SLC15A1, SNORD13G, 162 more genes
    nsv3919227copy number variation1nstd102humanPathogenic GRCh37 chr13: 97,866,125-109,815,264 , NCBI36 chr13: 96,664,126-108,613,265 , GRCh38 chr13: 97,213,871-109,162,916 SLC15A1, LINC00443, 147 more genes
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