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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5971473inversion1nstd209human GRCh38 chr5: 155,906,898-156,286,833 , GRCh37.p13 chr5: 155,333,908-155,713,843 SGCD
    nsv5967195insertion1nstd209human GRCh38 chr5: 156,653,493-156,653,493 , GRCh37.p13 chr5: 156,080,504-156,080,504 SGCD
    nsv5966555insertion1nstd209human GRCh38 chr5: 156,350,247-156,350,247 , GRCh37.p13 chr5: 155,777,257-155,777,257 SGCD
    nsv5964132insertion1nstd209human GRCh38 chr5: 156,471,927-156,471,927 , GRCh37.p13 chr5: 155,898,937-155,898,937 SGCD
    nsv5963712insertion1nstd209human GRCh38 chr5: 156,185,849-156,185,849 , GRCh37.p13 chr5: 155,612,859-155,612,859 SGCD
    nsv5957218insertion1nstd209human GRCh38 chr5: 155,863,603-155,863,603 , GRCh37.p13 chr5: 155,290,613-155,290,613 SGCD
    nsv5955954insertion1nstd209human GRCh38 chr5: 155,873,223-155,873,223 , GRCh37.p13 chr5: 155,300,233-155,300,233 SGCD
    nsv5953775insertion1nstd209human GRCh38 chr5: 156,307,554-156,307,554 , GRCh37.p13 chr5: 155,734,564-155,734,564 SGCD
    nsv5953603insertion1nstd209human GRCh38 chr5: 155,753,313-155,753,313 , GRCh37.p13 chr5: 155,132,873-155,132,873 SGCD
    nsv5949934insertion1nstd209human GRCh38 chr5: 156,192,854-156,192,854 , GRCh37.p13 chr5: 155,619,864-155,619,864 SGCD
    nsv5947604insertion1nstd209human GRCh38 chr5: 156,056,645-156,056,645 , GRCh37.p13 chr5: 155,483,655-155,483,655 SGCD
    nsv5906664copy number variation1nstd209human GRCh38 chr5: 156,228,804-156,228,881 , GRCh37.p13 chr5: 155,655,814-155,655,891 SGCD
    nsv5906510copy number variation1nstd209human GRCh38 chr5: 156,483,552-156,484,641 , GRCh37.p13 chr5: 155,910,562-155,911,651 SGCD
    nsv5906379copy number variation1nstd209human GRCh38 chr5: 155,925,035-155,925,116 , GRCh37.p13 chr5: 155,352,045-155,352,126 SGCD
    nsv5905065copy number variation1nstd209human GRCh38 chr5: 155,801,763-155,802,013 , GRCh37.p13 chr5: 155,228,773-155,229,023 SGCD
    nsv5903835copy number variation1nstd209human GRCh38 chr5: 156,082,539-156,082,596 , GRCh37.p13 chr5: 155,509,549-155,509,606 SGCD
    nsv5903262copy number variation1nstd209human GRCh38 chr5: 155,853,101-155,853,155 , GRCh37.p13 chr5: 155,280,111-155,280,165 SGCD
    nsv5901769copy number variation1nstd209human GRCh38 chr5: 156,039,289-156,039,368 , GRCh37.p13 chr5: 155,466,299-155,466,378 SGCD
    nsv5900729copy number variation1nstd209human GRCh38 chr5: 155,760,266-155,761,323 , GRCh37.p13 chr: NaN-NaN SGCD
    nsv5899659copy number variation1nstd209human GRCh38 chr5: 156,741,516-156,741,572 , GRCh37.p13 chr5: 156,168,527-156,168,583 LOC105377673, SGCD
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