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Items: 1 to 20 of 309

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5918566copy number variation1nstd209human GRCh38 chr9: 15,488,092-15,488,782 , GRCh37.p13 chr9: 15,488,090-15,488,780 PSIP1
    nsv5916583copy number variation1nstd209human GRCh38 chr9: 15,474,543-15,474,839 , GRCh37.p13 chr9: 15,474,541-15,474,837 PSIP1
    nsv5629293insertion1nstd207human GRCh38 chr9: 15,488,804-15,488,804 , GRCh37.p13 chr9: 15,488,802-15,488,802 PSIP1
    nsv5553878insertion1nstd206human GRCh38 chr9: 15,477,500-15,477,530 , GRCh37.p13 chr9: 15,477,498-15,477,528 PSIP1
    nsv5483195copy number variation1nstd206human GRCh38 chr9: 15,474,543-15,474,840 , GRCh37.p13 chr9: 15,474,541-15,474,838 PSIP1
    nsv5478904copy number variation1nstd206human GRCh38 chr9: 15,488,841-15,489,517 , GRCh37.p13 chr9: 15,488,839-15,489,515 PSIP1
    nsv5381767copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,654,812 , GRCh38.p12 chr9: 204,193-18,654,814 ACTG1P14, DMAC1, 191 more genes
    nsv5364692translocation1nstd200human GRCh38 chr9: 15,474,543-15,474,543 , GRCh38 chr9: 15,474,840-15,474,840 , GRCh37.p13 chr9: 15,474,541-15,474,541 , GRCh37.p13 chr9: 15,474,838-15,474,838 PSIP1
    nsv5040090inversion1nstd200human GRCh38 chr9: 12,646,715-21,082,031 , GRCh37.p13 chr9: 12,646,715-21,082,030 , RPS6, 98 more genes
    nsv4969381copy number variation1nstd200human GRCh38 chr9: 15,246,386-15,506,731 , GRCh37.p13 chr9: 15,246,384-15,506,729 RNU6-319P, RPL7P33, 3 more genes
    nsv4968273copy number variation1nstd200human GRCh38 chr9: 15,501,833-15,504,350 , GRCh37.p13 chr9: 15,501,831-15,504,348 PSIP1
    nsv4968272copy number variation1nstd200human GRCh38 chr9: 15,494,469-15,504,602 , GRCh37.p13 chr9: 15,494,467-15,504,600 PSIP1
    nsv4968271copy number variation1nstd200human GRCh38 chr9: 15,488,111-15,489,347 , GRCh37.p13 chr9: 15,488,109-15,489,345 PSIP1
    nsv4952856copy number variation1nstd200human GRCh38 chr9: 15,401,634-15,462,924 , GRCh37.p13 chr9: 15,401,632-15,462,922 PSIP1, RNU6-319P, 1 more genes
    nsv4823651copy number variation1nstd200human GRCh37 chr9: 15,501,831-15,504,348 , GRCh38.p12 chr9: 15,501,833-15,504,350 PSIP1
    nsv4823650copy number variation1nstd200human GRCh37 chr9: 15,488,109-15,489,345 , GRCh38.p12 chr9: 15,488,111-15,489,347 PSIP1
    nsv4823649copy number variation1nstd200human GRCh37 chr9: 15,488,120-15,488,843 , GRCh38.p12 chr9: 15,488,122-15,488,845 PSIP1
    nsv4814652copy number variation1nstd200human GRCh37 chr9: 15,246,384-15,506,729 , GRCh38.p12 chr9: 15,246,386-15,506,731 SNAPC3, RNU6-319P, 3 more genes
    nsv4768366copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,073,357 , GRCh38.p12 chr9: 204,193-18,073,359 DOCK8-AS1, RN7SL25P, 186 more genes
    nsv4768365copy number variation1nstd102humanPathogenic GRCh37 chr9: 13,638,428-17,121,764 , GRCh38.p12 chr9: 13,638,429-17,121,766 LINC03041, LINC00583, 38 more genes
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