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Items: 1 to 20 of 1269

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv4006789copy number variation1estd231human GRCh37 chr4: 89,681,460-89,681,782 , GRCh38.p12 chr4: 88,760,309-88,760,631 FAM13A
    nsv6752572copy number variation1nstd229human GRCh38 chr4: 88,986,180-89,024,842 , GRCh37.p13 chr4: 89,907,331-89,945,993 FAM13A
    nsv6757147copy number variation1nstd229human GRCh38 chr4: 89,067,093-89,078,175 , GRCh37.p13 chr4: 89,988,244-89,999,326 FAM13A
    nsv6746276copy number variation1nstd229human GRCh38 chr4: 88,893,988-88,901,013 , GRCh37.p13 chr4: 89,815,139-89,822,164 FAM13A
    nsv6743917copy number variation1nstd229human GRCh38 chr4: 88,899,954-88,906,329 , GRCh37.p13 chr4: 89,821,105-89,827,480 FAM13A
    nsv6752999copy number variation1nstd229human GRCh38 chr4: 89,044,670-89,049,403 , GRCh37.p13 chr4: 89,965,821-89,970,554 FAM13A
    nsv6757810copy number variation1nstd229human GRCh38 chr4: 88,968,427-88,972,999 , GRCh37.p13 chr4: 89,889,578-89,894,150 FAM13A
    nsv6748486copy number variation1nstd229human GRCh38 chr4: 89,043,932-89,047,967 , GRCh37.p13 chr4: 89,965,083-89,969,118 FAM13A
    nsv6747255copy number variation1nstd229human GRCh38 chr4: 88,864,980-88,868,630 , GRCh37.p13 chr4: 89,786,131-89,789,781 FAM13A
    nsv6754647copy number variation1nstd229human GRCh38 chr4: 88,799,821-88,803,101 , GRCh37.p13 chr4: 89,720,972-89,724,252 FAM13A
    nsv6757903copy number variation1nstd229human GRCh38 chr4: 89,083,212-89,086,338 , GRCh37.p13 chr4: 90,004,363-90,007,489 FAM13A
    nsv6754554copy number variation1nstd229human GRCh38 chr4: 88,998,900-89,001,766 , GRCh37.p13 chr4: 89,920,051-89,922,917 FAM13A
    nsv6744233copy number variation1nstd229human GRCh38 chr4: 88,716,456-88,719,200 , GRCh37.p13 chr4: 89,637,607-89,640,351 FAM13A-AS1
    nsv6749159copy number variation1nstd229human GRCh38 chr4: 88,869,540-88,871,457 , GRCh37.p13 chr4: 89,790,691-89,792,608 FAM13A
    nsv6749018copy number variation1nstd229human GRCh38 chr4: 88,904,130-88,905,821 , GRCh37.p13 chr4: 89,825,281-89,826,972 FAM13A
    nsv6746470copy number variation1nstd229human GRCh38 chr4: 88,733,700-88,734,263 , GRCh37.p13 chr4: 89,654,851-89,655,414 FAM13A
    nsv6756734copy number variation1nstd229human GRCh38 chr4: 88,999,786-89,000,138 , GRCh37.p13 chr4: 89,920,937-89,921,289 FAM13A
    nsv6755687copy number variation1nstd229human GRCh38 chr4: 88,760,322-88,760,631 , GRCh37.p13 chr4: 89,681,473-89,681,782 FAM13A
    nsv6743957copy number variation1nstd229human GRCh38 chr4: 89,077,784-89,077,830 , GRCh37.p13 chr4: 89,998,935-89,998,981 FAM13A
    nsv6741828copy number variation1nstd229human GRCh38 chr4: 88,912,221-88,912,266 , GRCh37.p13 chr4: 89,833,372-89,833,417 FAM13A
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