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Items: 1 to 20 of 195

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5896065copy number variation1nstd209human GRCh38 chr5: 140,624,747-140,626,770 , GRCh37.p13 chr5: 140,004,332-140,006,355 TMCO6
    nsv5691027mobile element insertion1nstd211human GRCh38 chr5: 140,609,444-140,609,444 , GRCh37.p13 chr5: 139,989,029-139,989,029 RPL36P11, TMCO6
    nsv5676693mobile element insertion1nstd211human GRCh38 chr5: 140,609,428-140,609,428 , GRCh37.p13 chr5: 139,989,013-139,989,013 RPL36P11, TMCO6
    nsv5633557insertion1nstd207human GRCh38 chr5: 140,637,974-140,637,974 , GRCh37.p13 chr5: 140,017,559-140,017,559 TMCO6
    nsv5465641copy number variation1nstd206human GRCh38 chr5: 140,624,533-140,626,644 , GRCh37.p13 chr5: 140,004,118-140,006,229 TMCO6
    nsv5459852copy number variation1nstd206human GRCh38 chr5: 140,600,020-140,600,075 , GRCh37.p13 chr5: 139,979,605-139,979,660 TMCO6
    nsv5454825copy number variation1nstd206human GRCh38 chr5: 140,633,060-140,633,964 , GRCh37.p13 chr5: 140,012,645-140,013,549 TMCO6, CD14
    nsv5409460mobile element insertion1nstd206human GRCh38 chr5: 140,609,444-140,609,495 , GRCh37.p13 chr5: 139,989,029-139,989,080 RPL36P11, TMCO6
    nsv5381510copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,633,338-140,998,481 , GRCh38.p12 chr5: 137,297,649-141,618,914 RNA5SP195, LOC112267855, 174 more genes
    nsv5314979copy number variation1nstd204human GRCh38.p13 chr5: 140,624,623-140,626,580 , GRCh37.p13 chr5: 140,004,208-140,006,165 TMCO6
    nsv5239279copy number variation1nstd204human GRCh38.p13 chr5: 140,624,701-140,628,600 , GRCh37.p13 chr5: 140,004,286-140,008,185 TMCO6
    nsv5098221mobile element insertion1nstd203human GRCh38 chr5: 140,608,443-140,608,459 , GRCh37.p13 chr5: 139,988,028-139,988,044 RPL36P11, TMCO6
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4938913copy number variation1nstd200human GRCh38 chr5: 140,635,007-140,636,196 , GRCh37.p13 chr5: 140,014,592-140,015,781 TMCO6
    nsv4938912copy number variation1nstd200human GRCh38 chr5: 140,633,327-140,634,290 , GRCh37.p13 chr5: 140,012,912-140,013,875 TMCO6, CD14
    nsv4938911copy number variation1nstd200human GRCh38 chr5: 140,612,552-140,614,741 , GRCh37.p13 chr5: 139,992,137-139,994,326 TMCO6
    nsv4938910copy number variation1nstd200human GRCh38 chr5: 140,607,669-140,607,948 , GRCh37.p13 chr5: 139,987,254-139,987,533 TMCO6, RPL36P11
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4805867copy number variation1nstd200human GRCh37 chr5: 140,004,215-140,006,444 , GRCh38.p12 chr5: 140,624,630-140,626,859 TMCO6
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