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Items: 1 to 20 of 107

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4456376copy number variation1nstd102humanUncertain significance GRCh37 chr13: 111,846,270-111,877,000 , GRCh38.p12 chr13: 111,193,923-111,224,653 ARHGEF7
    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 ARHGEF7, 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 ARHGEF7, LOC105370271, 925 more genes
    nsv4675850copy number variation1nstd102humanPathogenic GRCh37 chr13: 53,262,013-115,107,733 , GRCh38.p12 chr13: 52,687,878-114,342,258 ARHGEF7, TEX30, 680 more genes
    nsv6314171copy number variation1nstd102humanPathogenic GRCh37 chr13: 79,370,012-115,107,733 , GRCh38.p12 chr13: 78,795,877-114,342,258 ARHGEF7, MIR4705, 430 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 ARHGEF7, LOC107984609, 369 more genes
    nsv3903376copy number variation1nstd102humanPathogenic GRCh37 chr13: 88,073,140-115,107,733 , GRCh38.p12 chr13: 87,420,885-114,342,258 ARHGEF7, ZIC2, 364 more genes
    nsv3896487copy number variation1nstd102humanPathogenic GRCh37 chr13: 89,796,110-115,083,342 , GRCh38.p12 chr13: 89,143,856-114,317,867 ARHGEF7, TMTC4, 347 more genes
    nsv3890560copy number variation1nstd102humanPathogenic GRCh37 chr13: 94,474,530-115,107,733 , GRCh38.p12 chr13: 93,822,277-114,342,258 ARHGEF7, RPL15P18, 303 more genes
    nsv3892450copy number variation1nstd102humanPathogenic GRCh37 chr13: 96,586,481-115,107,733 , GRCh38.p12 chr13: 95,934,227-114,342,258 ARHGEF7, RPS6P23, 268 more genes
    nsv4675644copy number variation1nstd102humanPathogenic GRCh37 chr13: 96,895,656-115,107,733 , GRCh38.p12 chr13: 96,243,402-114,342,258 ARHGEF7, ZIC2, 266 more genes
    nsv6637400copy number variation1nstd102humanPathogenic GRCh37 chr13: 97,142,120-115,107,733 , GRCh38.p12 chr13: 96,489,866-114,342,258 ARHGEF7, LOC107984609, 265 more genes
    nsv6314066copy number variation1nstd102humanPathogenic GRCh37 chr13: 100,258,328-115,107,733 , GRCh38.p12 chr13: 99,606,074-114,342,258 ARHGEF7, MIR4502, 208 more genes
    nsv3905010copy number variation1nstd102humanPathogenic GRCh37 chr13: 101,075,864-115,105,020 , GRCh38.p12 chr13: 100,423,610-114,339,545 ARHGEF7, RN7SKP10, 194 more genes
    nsv4728419copy number variation1nstd102humanPathogenic GRCh37 chr13: 102,175,801-115,169,858 , GRCh38.p12 chr13: 101,523,450-114,344,403 ARHGEF7, RPL7P45, 182 more genes
    nsv3916756copy number variation1nstd102humanPathogenic NCBI36 chr13: 100,987,397-114,110,750 , GRCh38 chr13: 101,537,045-114,327,173 , GRCh37 chr13: 102,189,396-115,085,141 ARHGEF7, PROZ, 180 more genes
    nsv3913569copy number variation1nstd102humanPathogenic GRCh37 chr13: 102,766,375-115,085,141 , GRCh38 chr13: 102,114,025-114,327,173 , NCBI36 chr13: 101,564,376-114,110,750 ARHGEF7, TPP2, 172 more genes
    nsv3905205copy number variation1nstd102humanPathogenic GRCh37 chr13: 103,170,306-115,107,733 , GRCh38.p12 chr13: 102,517,956-114,342,258 ARHGEF7, MIR548AR, 168 more genes
    nsv3922934copy number variation1nstd102humanPathogenic GRCh37 chr13: 103,535,672-115,085,141 , NCBI36 chr13: 102,333,673-114,123,908 , GRCh38 chr13: 102,883,322-114,340,331 ARHGEF7, LINC01054, 157 more genes
    nsv3905783copy number variation1nstd102humanPathogenic GRCh37 chr13: 103,880,953-115,107,733 , GRCh38.p12 chr13: 103,228,603-114,342,258 ARHGEF7, LOC105370372, 155 more genes
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