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Items: 1 to 20 of 312

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7090437copy number variation1nstd229human GRCh38 chrX: 100,819,196-100,819,533 , GRCh37.p13 chrX: 100,074,185-100,074,522 CSTF2
    nsv3959634insertion1nstd168human GRCh38 chrX: 100,822,408-100,825,938 , GRCh37.p13 chrX: 100,077,397-100,080,927 CSTF2
    esv2342108insertion1estd194human NCBI36 chrX: 99,976,922-99,976,922 , GRCh37.p13 chrX: 100,090,266-100,090,266 , GRCh38.p12 chrX: 100,835,277-100,835,277 CSTF2
    nsv423882insertion1nstd6human NCBI35 chrX: 99,896,694-99,896,694 , GRCh37.p13 chrX: 100,090,549-100,090,549 , GRCh38.p12 chrX: 100,835,560-100,835,560 CSTF2
    nsv419502insertion1nstd6human NCBI35 chrX: 99,887,436-99,887,436 , GRCh37.p13 chrX: 100,081,291-100,081,291 , GRCh38.p12 chrX: 100,826,302-100,826,302 CSTF2
    nsv418441insertion1nstd6human NCBI35 chrX: 99,896,692-99,896,692 , GRCh37.p13 chrX: 100,090,547-100,090,547 , GRCh38.p12 chrX: 100,835,558-100,835,558 CSTF2
    nsv2681235short tandem repeat2nstd128human GRCh37 chrX: 100,093,029-100,093,053 , GRCh38.p12 chrX: 100,838,040-100,838,064 CSTF2
    nsv2681234short tandem repeat1nstd128human GRCh37 chrX: 100,080,225-100,080,248 , GRCh38.p12 chrX: 100,825,236-100,825,259 CSTF2
    nsv2680453short tandem repeat1nstd128human GRCh37 chrX: 100,084,519-100,084,537 , GRCh38.p12 chrX: 100,829,530-100,829,548 CSTF2
    nsv2700579short tandem repeat1nstd128human GRCh37 chrX: 100,087,212-100,087,227 , GRCh38.p12 chrX: 100,832,223-100,832,238 CSTF2
    nsv2700576short tandem repeat1nstd128human GRCh37 chrX: 100,075,938-100,075,953 , GRCh38.p12 chrX: 100,820,949-100,820,964 CSTF2
    nsv2700578short tandem repeat2nstd128human GRCh37 chrX: 100,084,499-100,084,513 , GRCh38.p12 chrX: 100,829,510-100,829,524 CSTF2
    nsv2681233short tandem repeat7nstd128human GRCh37 chrX: 100,077,085-100,077,099 , GRCh38.p12 chrX: 100,822,096-100,822,110 CSTF2
    nsv2680454short tandem repeat7nstd128human GRCh37 chrX: 100,090,266-100,090,280 , GRCh38.p12 chrX: 100,835,277-100,835,291 CSTF2
    nsv2700580short tandem repeat4nstd128human GRCh37 chrX: 100,090,537-100,090,548 , GRCh38.p12 chrX: 100,835,548-100,835,559 CSTF2
    nsv4374649copy number variation1nstd173human GRCh37 chrX: 100,078,029-100,103,688 , GRCh38.p12 chrX: 100,823,040-100,848,699 CSTF2, NOX1
    esv3240998copy number variation1estd209human GRCh37 chrX: 100,098,355-100,098,358 , GRCh38.p12 chrX: 100,843,366-100,843,369 CSTF2, NOX1
    esv1409050copy number variation1estd22human NCBI36 chrX: 99,985,013-99,985,016 , GRCh37.p13 chrX: 100,098,357-100,098,360 , GRCh38.p12 chrX: 100,843,368-100,843,371 CSTF2, NOX1
    nsv7090438copy number variation1nstd229human GRCh38 chrX: 100,819,201-100,844,700 , GRCh37.p13 chrX: 100,074,190-100,099,689 CSTF2, NOX1
    nsv5364245translocation1nstd200human GRCh38 chrX: 100,838,935-100,838,935 , GRCh38 chr8: 73,945,612-73,945,612 , GRCh37.p13 chrX: 100,093,924-100,093,924 , GRCh37.p13 chr8: 74,857,847-74,857,847 CSTF2, ELOC
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