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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977899inversion1nstd209human GRCh38 chr2: 227,539,323-230,369,909 , GRCh37.p13 chr2: 228,404,039-231,234,624 , AGFG1, 40 more genes
    nsv5687670mobile element insertion1nstd211human GRCh38 chr2: 230,166,560-230,166,560 , GRCh37.p13 chr2: 231,031,276-231,031,276 SP110
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5449024copy number variation1nstd206human GRCh38 chr2: 228,447,618-230,410,000 , GRCh37.p13 chr2: 229,312,334-231,274,715 , RPL7L1P10, 25 more genes
    nsv5434386copy number variation1nstd206human GRCh38 chr2: 230,164,778-230,165,675 , GRCh37.p13 chr2: 231,029,494-231,030,391 SP110
    nsv5351183translocation1nstd200human GRCh38 chr2: 230,206,567-230,206,567 , GRCh38 chr2: 230,206,634-230,206,634 , GRCh37.p13 chr2: 231,071,282-231,071,282 , GRCh37.p13 chr2: 231,071,349-231,071,349 SP110, SP140
    nsv5314204copy number variation1nstd204human GRCh37.p13 chr2: 231,071,250-231,075,896 , GRCh38.p13 chr2: 230,206,535-230,211,181 SP110, SP140
    nsv5309322copy number variation1nstd204human GRCh37.p13 chr2: 231,068,226-231,070,733 , GRCh38.p13 chr2: 230,203,510-230,206,018 SP110, SP140
    nsv5200403copy number variation1nstd204human GRCh38.p13 chr2: 230,203,476-230,210,754 , GRCh37.p13 chr2: 231,068,192-231,075,469 SP140, SP110
    nsv5064146mobile element insertion1nstd203human GRCh38 chr2: 230,187,064-230,187,076 , GRCh37.p13 chr2: 231,051,780-231,051,792 SP110
    nsv5039254inversion1nstd200human GRCh38 chr2: 227,539,122-230,370,113 , GRCh37.p13 chr2: 228,403,838-231,234,828 , LOC105373921, 40 more genes
    nsv4917314copy number variation1nstd200human GRCh38 chr2: 230,183,735-230,190,357 , GRCh37.p13 chr2: 231,048,451-231,055,073 SP110
    nsv4917313copy number variation1nstd200human GRCh38 chr2: 230,176,013-230,177,979 , GRCh37.p13 chr2: 231,040,729-231,042,695 SP110
    nsv4914028copy number variation1nstd200human GRCh38 chr2: 230,180,467-230,272,344 , GRCh37.p13 chr2: 231,045,183-231,137,059 SP110, SP140
    nsv4806207copy number variation1nstd200human GRCh37 chr2: 231,071,260-231,075,888 , GRCh38.p12 chr2: 230,206,545-230,211,173 SP140, SP110
    nsv4806206copy number variation1nstd200human GRCh37 chr2: 231,068,236-231,070,731 , GRCh38.p12 chr2: 230,203,520-230,206,016 SP140, SP110
    nsv4806205copy number variation1nstd200human GRCh37 chr2: 231,048,450-231,055,073 , GRCh38.p12 chr2: 230,183,734-230,190,357 SP110
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 LOC105376755, FZD7, 1013 more genes
    nsv4682883copy number variation1nstd102humanUncertain significance GRCh37 chr2: 231,048,268-231,086,456 , GRCh38.p12 chr2: 230,183,552-230,221,741 SP140, SP110
    nsv4681333copy number variation1nstd102humanPathogenic GRCh37 chr2: 231,041,361-231,042,416 , GRCh38.p12 chr2: 230,176,645-230,177,700 SP110
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