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Items: 1 to 20 of 134

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6287008insertion1nstd214human GRCh38 chr13: 18,232,373-18,232,373 , GRCh37.p13 chrUn|NT_113923.1: 61,125-61,125 FAM230C
    nsv6272257copy number variation1nstd214human GRCh38 chr13: 18,198,435-18,198,490 , GRCh37.p13 chrUn|NT_113923.1: 27,187-27,242 FAM230C
    nsv6248747mobile element insertion1nstd215human GRCh38 chr13: 18,196,956-18,196,956 , GRCh37.p13 chrUn|NT_113923.1: 25,708-25,708 FAM230C
    nsv6203483copy number variation1nstd214human GRCh38 chr13: 18,232,434-18,232,487 , GRCh37.p13 chrUn|NT_113923.1: 61,186-61,239 FAM230C
    nsv6098209insertion1nstd212human GRCh38 chr13: 18,212,712-18,212,712 , GRCh37.p13 chrUn|NT_113923.1: 41,464-41,464 FAM230C
    nsv6096244insertion1nstd212human GRCh38 chr13: 18,214,071-18,214,071 , GRCh37.p13 chrUn|NT_113923.1: 42,823-42,823 FAM230C
    nsv6095572insertion1nstd212human GRCh38 chr13: 18,211,223-18,211,223 , GRCh37.p13 chrUn|NT_113923.1: 39,975-39,975 FAM230C
    nsv6094482insertion1nstd212human GRCh38 chr13: 18,196,940-18,196,940 , GRCh37.p13 chrUn|NT_113923.1: 25,692-25,692 FAM230C
    nsv6089963insertion1nstd212human GRCh38 chr13: 18,211,710-18,211,710 , GRCh37.p13 chrUn|NT_113923.1: 40,462-40,462 FAM230C
    nsv6088036insertion1nstd212human GRCh38 chr13: 18,214,814-18,214,814 , GRCh37.p13 chrUn|NT_113923.1: 43,566-43,566 FAM230C
    nsv6083384insertion1nstd212human GRCh38 chr13: 18,215,498-18,215,498 , GRCh37.p13 chrUn|NT_113923.1: 44,250-44,250 FAM230C
    nsv6081578insertion1nstd212human GRCh38 chr13: 18,212,717-18,212,717 , GRCh37.p13 chrUn|NT_113923.1: 41,469-41,469 FAM230C
    nsv6039268copy number variation1nstd212human GRCh38 chr13: 18,213,025-18,213,568 , GRCh37.p13 chrUn|NT_113923.1: 41,777-42,320 FAM230C
    nsv6039121copy number variation1nstd212human GRCh38 chr13: 18,212,562-18,212,933 , GRCh37.p13 chrUn|NT_113923.1: 41,314-41,685 FAM230C
    nsv6038652copy number variation1nstd212human GRCh38 chr13: 18,198,416-18,198,590 , GRCh37.p13 chrUn|NT_113923.1: 27,168-27,342 FAM230C
    nsv6036049copy number variation1nstd212human GRCh38 chr13: 18,213,521-18,213,807 , GRCh37.p13 chrUn|NT_113923.1: 42,273-42,559 FAM230C
    nsv6032133copy number variation1nstd212human GRCh38 chr13: 18,198,435-18,198,491 , GRCh37.p13 chrUn|NT_113923.1: 27,187-27,243 FAM230C
    nsv6025064copy number variation1nstd212human GRCh38 chr13: 18,212,566-18,214,351 , GRCh37.p13 chrUn|NT_113923.1: 41,318-43,103 FAM230C
    nsv6023465copy number variation1nstd212human GRCh38 chr13: 18,213,009-18,213,239 , GRCh37.p13 chrUn|NT_113923.1: 41,761-41,991 FAM230C
    nsv6022989copy number variation1nstd212human GRCh38 chr13: 18,213,867-18,214,139 , GRCh37.p13 chrUn|NT_113923.1: 42,619-42,891 FAM230C
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