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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142444copy number variation1nstd232human GRCh37.p13 chr11: 16,905,547-16,905,599 , GRCh38.p12 chr11: 16,884,000-16,884,052 PLEKHA7
    nsv7137744copy number variation1nstd232human GRCh37.p13 chr11: 16,928,660-16,928,757 , GRCh38.p12 chr11: 16,907,113-16,907,210 PLEKHA7
    nsv7074937inversion1nstd229human GRCh38 chr11: 16,856,160-16,860,780 , GRCh37.p13 chr11: 16,877,707-16,882,327 PLEKHA7
    nsv7073121inversion1nstd229human GRCh38 chr11: 16,776,341-16,780,559 , GRCh37.p13 chr11: 16,797,888-16,802,106 PLEKHA7
    nsv7071778inversion1nstd229human GRCh38 chr11: 16,974,009-16,974,143 , GRCh37.p13 chr11: 16,995,556-16,995,690 RPL36AP37, PLEKHA7
    nsv7070030inversion1nstd229human GRCh38 chr11: 16,966,270-21,356,221 , GRCh37.p13 chr11: 16,987,817-21,377,767 DBX1, PRMT3, 93 more genes
    nsv7059267inversion1nstd229human GRCh38 chr11: 16,772,650-16,776,825 , GRCh37.p13 chr11: 16,794,197-16,798,372 PLEKHA7
    nsv7058428inversion1nstd229human GRCh38 chr11: 14,504,801-17,598,701 , GRCh37.p13 chr11: 14,526,347-17,620,248 RPL36AP37, LOC105376567, 41 more genes
    nsv6917622copy number variation1nstd229human GRCh38 chr11: 16,849,235-16,849,832 , GRCh37.p13 chr11: 16,870,782-16,871,379 PLEKHA7
    nsv6917151copy number variation1nstd229human GRCh38 chr11: 9,940,109-18,580,574 , GRCh37.p13 chr11: 9,961,656-18,602,121 MYOD1, MIR8070, 139 more genes
    nsv6916951copy number variation1nstd229human GRCh38 chr11: 16,805,867-16,808,796 , GRCh37.p13 chr11: 16,827,414-16,830,343 PLEKHA7
    nsv6916062copy number variation1nstd229human GRCh38 chr11: 16,953,022-16,962,292 , GRCh37.p13 chr11: 16,974,569-16,983,839 PLEKHA7
    nsv6915189copy number variation1nstd229human GRCh38 chr11: 16,827,114-16,831,717 , GRCh37.p13 chr11: 16,848,661-16,853,264 PLEKHA7
    nsv6914529copy number variation1nstd229human GRCh38 chr11: 16,793,016-16,796,419 , GRCh37.p13 chr11: 16,814,563-16,817,966 PLEKHA7
    nsv6913770copy number variation1nstd229human GRCh38 chr11: 16,874,077-16,874,149 , GRCh37.p13 chr11: 16,895,624-16,895,696 PLEKHA7
    nsv6910385copy number variation1nstd229human GRCh38 chr11: 16,804,550-16,804,741 , GRCh37.p13 chr11: 16,826,097-16,826,288 PLEKHA7
    nsv6909872copy number variation1nstd229human GRCh38 chr11: 16,870,318-16,883,397 , GRCh37.p13 chr11: 16,891,865-16,904,944 PLEKHA7
    nsv6909592copy number variation1nstd229human GRCh38 chr11: 16,818,988-16,819,545 , GRCh37.p13 chr11: 16,840,535-16,841,092 PLEKHA7
    nsv6908649copy number variation1nstd229human GRCh38 chr11: 16,928,007-16,931,646 , GRCh37.p13 chr11: 16,949,554-16,953,193 PLEKHA7
    nsv6908228copy number variation1nstd229human GRCh38 chr11: 16,997,689-17,003,382 , GRCh37.p13 chr11: 17,019,236-17,024,929 PLEKHA7
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