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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7078008inversion1nstd229human GRCh38 chr14: 60,214,891-67,756,686 , GRCh37.p13 chr14: 60,681,609-68,223,403 ATP6V1D, LOC101927756, 129 more genes
    nsv7077538inversion1nstd229human GRCh38 chr14: 63,703,374-67,849,523 , GRCh37.p13 chr14: 64,170,092-68,316,240 RPPH1-2P, SYNE2, 75 more genes
    nsv7077051inversion1nstd229human GRCh38 chr14: 63,334,072-65,942,752 , GRCh37.p13 chr14: 63,800,790-66,409,470 FNTB, PPP1R36, 53 more genes
    nsv7059243inversion1nstd229human GRCh38 chr14: 63,034,368-65,530,331 , GRCh37.p13 chr14: 63,501,086-65,997,049 MIR4706, RNU7-116P, 56 more genes
    nsv6977506copy number variation1nstd229human GRCh38 chr14: 62,671,855-65,773,169 , GRCh37.p13 chr14: 63,138,573-66,239,887 KCNH5, CHURC1-FNTB, 56 more genes
    nsv6976248copy number variation1nstd229human GRCh38 chr14: 64,725,732-64,725,784 , GRCh37.p13 chr14: 65,192,450-65,192,502 PLEKHG3
    nsv6971674copy number variation1nstd229human GRCh38 chr14: 64,748,166-64,748,261 , GRCh37.p13 chr14: 65,214,884-65,214,979 PLEKHG3, SPTB
    nsv6970709copy number variation1nstd229human GRCh38 chr14: 64,692,012-64,744,230 , GRCh37.p13 chr14: 65,158,730-65,210,948 SPTB, PLEKHG3
    nsv6965760copy number variation1nstd229human GRCh38 chr14: 64,726,123-64,729,350 , GRCh37.p13 chr14: 65,192,841-65,196,068 PLEKHG3
    nsv6965189copy number variation1nstd229human GRCh38 chr14: 64,722,578-64,726,010 , GRCh37.p13 chr14: 65,189,296-65,192,728 PLEKHG3
    nsv6961833copy number variation1nstd229human GRCh38 chr14: 64,698,436-64,703,560 , GRCh37.p13 chr14: 65,165,154-65,170,278 PLEKHG3
    nsv6961542copy number variation1nstd229human GRCh38 chr14: 64,745,183-64,751,909 , GRCh37.p13 chr14: 65,211,901-65,218,627 SPTB, PLEKHG3
    nsv6960520copy number variation1nstd229human GRCh38 chr14: 64,700,079-65,240,524 , GRCh37.p13 chr14: 65,166,797-65,707,242 MAX, LINC02324, 15 more genes
    nsv6492638copy number variation1nstd223human GRCh38 chr14: 64,733,079-64,735,494 , GRCh37.p13 chr14: 65,199,797-65,202,212 PLEKHG3
    nsv6490099copy number variation1nstd223human GRCh38 chr14: 64,748,163-64,748,261 , GRCh37.p13 chr14: 65,214,881-65,214,979 SPTB, PLEKHG3
    nsv6484071copy number variation1nstd223human GRCh38 chr14: 64,726,123-64,729,350 , GRCh37.p13 chr14: 65,192,841-65,196,068 PLEKHG3
    nsv6476063copy number variation1nstd223human GRCh38 chr14: 64,354,345-74,200,229 , GRCh37.p13 chr14: 64,821,063-74,666,932 RNU6-240P, COX7A2P1, 196 more genes
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 PAPOLA-DT, LOC105378180, 1338 more genes
    nsv6315477copy number variation1nstd102humanUncertain significance GRCh37 chr14: 64,016,496-65,834,490 , GRCh38.p12 chr14: 63,549,778-65,367,772 LOC105370534, RNU7-116P, 43 more genes
    nsv6271932copy number variation1nstd214human GRCh38 chr14: 64,748,163-64,748,260 , GRCh37.p13 chr14: 65,214,881-65,214,978 PLEKHG3, SPTB
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