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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3873515copy number variation1nstd102humanBenign GRCh37 chr6: 37,851,595-37,852,459 , GRCh38.p12 chr6: 37,883,819-37,884,683 ZFAND3
    esv4003175copy number variation1estd231human GRCh37 chr6: 37,851,224-37,852,576 , GRCh38.p12 chr6: 37,883,448-37,884,800 ZFAND3
    esv4007912copy number variation1estd231human GRCh37 chr6: 37,961,603-37,987,236 , GRCh38.p12 chr6: 37,993,827-38,019,460 ZFAND3
    nsv507324sequence alteration3nstd49human NCBI35 chr6: 38,157,957-38,163,957 , GRCh37.p13 chr6: 38,049,979-38,055,979 , GRCh38.p12 chr6: 38,082,203-38,088,203 ZFAND3
    nsv6797493copy number variation1nstd229human GRCh38 chr6: 37,842,103-37,903,291 , GRCh37.p13 chr6: 37,809,879-37,871,067 ZFAND3
    nsv6784780copy number variation1nstd229human GRCh38 chr6: 37,969,875-38,026,466 , GRCh37.p13 chr6: 37,937,651-37,994,242 ZFAND3
    nsv6784069copy number variation1nstd229human GRCh38 chr6: 38,003,723-38,041,223 , GRCh37.p13 chr6: 37,971,499-38,008,999 ZFAND3
    nsv6792945copy number variation1nstd229human GRCh38 chr6: 38,012,441-38,049,064 , GRCh37.p13 chr6: 37,980,217-38,016,840 ZFAND3
    nsv6789698copy number variation1nstd229human GRCh38 chr6: 37,937,034-37,973,008 , GRCh37.p13 chr6: 37,904,810-37,940,784 ZFAND3
    nsv6789608copy number variation1nstd229human GRCh38 chr6: 38,007,501-38,042,400 , GRCh37.p13 chr6: 37,975,277-38,010,176 ZFAND3
    nsv6782993copy number variation1nstd229human GRCh38 chr6: 37,965,786-38,000,369 , GRCh37.p13 chr6: 37,933,562-37,968,145 ZFAND3
    nsv6797039copy number variation1nstd229human GRCh38 chr6: 37,934,601-37,966,600 , GRCh37.p13 chr6: 37,902,377-37,934,376 ZFAND3
    nsv6797631copy number variation1nstd229human GRCh38 chr6: 37,966,558-37,990,385 , GRCh37.p13 chr6: 37,934,334-37,958,161 ZFAND3
    nsv6792169copy number variation1nstd229human GRCh38 chr6: 38,117,342-38,138,199 , GRCh37.p13 chr6: 38,085,118-38,105,975 ZFAND3
    nsv6792064copy number variation1nstd229human GRCh38 chr6: 37,989,301-38,002,200 , GRCh37.p13 chr6: 37,957,077-37,969,976 ZFAND3
    nsv6781739copy number variation1nstd229human GRCh38 chr6: 38,089,557-38,101,719 , GRCh37.p13 chr6: 38,057,333-38,069,495 ZFAND3
    nsv6791373copy number variation1nstd229human GRCh38 chr6: 38,033,890-38,044,273 , GRCh37.p13 chr6: 38,001,666-38,012,049 ZFAND3
    nsv6783212copy number variation1nstd229human GRCh38 chr6: 37,994,861-38,004,497 , GRCh37.p13 chr6: 37,962,637-37,972,273 ZFAND3
    nsv6792196copy number variation1nstd229human GRCh38 chr6: 37,967,552-37,975,923 , GRCh37.p13 chr6: 37,935,328-37,943,699 ZFAND3
    nsv6788297copy number variation1nstd229human GRCh38 chr6: 37,849,419-37,857,623 , GRCh37.p13 chr6: 37,817,195-37,825,399 ZFAND3
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