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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5429360copy number variation1nstd206human GRCh38 chr1: 111,687,835-115,150,000 , GRCh37.p13 chr1: 112,230,457-115,692,621 , ST7L, 77 more genes
    nsv5381058copy number variation1nstd102humanPathogenic GRCh37 chr1: 102,021,465-119,737,478 , GRCh38.p12 chr1: 101,555,909-119,194,855 AMYP1, MIR4256, 320 more genes
    nsv5363292translocation1nstd200human GRCh38 chr1: 112,718,098-112,718,098 , GRCh38 chr1: 112,703,510-112,703,510 , GRCh37.p13 chr1: 113,246,132-113,246,132 , GRCh37.p13 chr1: 113,260,720-113,260,720 RHOC, TAFA3, 1 more genes
    nsv5344222translocation1nstd200human GRCh37 chr1: 113,260,720-113,260,720 , GRCh37 chr1: 113,246,132-113,246,132 , GRCh38.p12 chr1: 112,718,098-112,718,098 , GRCh38.p12 chr1: 112,703,510-112,703,510 RHOC, TAFA3, 1 more genes
    nsv4894420copy number variation1nstd200human GRCh38 chr1: 112,702,675-113,232,556 , GRCh37.p13 chr1: 113,245,297-113,775,178 RHOC, RPS19P2, 19 more genes
    nsv4894419copy number variation1nstd200human GRCh38 chr1: 112,670,692-113,135,319 , GRCh37.p13 chr1: 113,213,314-113,677,941 CAPZA1, SLC16A1-AS1, 17 more genes
    nsv4894418copy number variation1nstd200human GRCh38 chr1: 112,549,341-113,353,065 , GRCh37.p13 chr1: 113,091,963-113,895,687 LOC105378911, RNU7-70P, 23 more genes
    nsv4890815copy number variation1nstd200human GRCh38 chr1: 112,706,049-112,706,192 , GRCh37.p13 chr1: 113,248,671-113,248,814 RHOC
    nsv4781125copy number variation1nstd200human GRCh37 chr1: 113,245,366-113,311,462 , GRCh38.p12 chr1: 112,702,744-112,768,840 NUTF2P4, PPM1J-DT, 4 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4761183inversion1nstd199human GRCh37 chr1: 16,884,570-145,374,569 , GRCh38.p12 chr1: 16,558,075-149,528,945 , ABCA4, 2341 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4745469copy number variation1nstd199human GRCh37 chr1: 86,005,697-146,486,085 , GRCh38.p12 chr1: 85,540,014-149,528,945 , TAF13, 920 more genes
    nsv4740962copy number variation1nstd199human GRCh37 chr1: 113,249,046-113,249,110 , GRCh38.p12 chr1: 112,706,424-112,706,488 RHOC
    nsv4664322copy number variation1nstd186human GRCh37 chr1: 112,692,629-113,246,263 , GRCh38.p12 chr1: 112,150,007-112,703,641 CTTNBP2NL, MRPL53P1, 9 more genes
    nsv4593815copy number variation1nstd183human GRCh37 chr1: 113,249,529-113,249,666 , GRCh38.p12 chr1: 112,706,907-112,707,044 RHOC
    nsv4593814copy number variation2nstd183human GRCh37 chr1: 113,246,318-113,350,775 , GRCh38.p12 chr1: 112,703,696-112,808,153 RHOC, PPM1J-DT, 3 more genes
    nsv4579101copy number variation1nstd183human GRCh37 chr1: 112,693,290-113,246,263 , GRCh38.p12 chr1: 112,150,668-112,703,641 LINC02884, RNU7-70P, 9 more genes
    nsv4579026copy number variation1nstd183human GRCh37 chr1: 113,249,529-113,249,814 , GRCh38.p12 chr1: 112,706,907-112,707,192 RHOC
    nsv4578768copy number variation1nstd183human GRCh37 chr1: 112,692,629-113,246,263 , GRCh38.p12 chr1: 112,150,007-112,703,641 ST7L, TXNP3, 9 more genes
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