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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096918copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr2: 7,968,276-10,192,634 , GRCh38.p12 chr2: 7,828,145-10,052,507 ITGB1BP1, LINC00299, 37 more genes
    nsv7056464inversion1nstd229human GRCh38 chr2: 8,910,932-8,917,687 , GRCh37.p13 chr2: 9,051,062-9,057,817 MBOAT2
    nsv7044096inversion1nstd229human GRCh38 chr2: 5,896,641-9,131,731 , GRCh37.p13 chr2: 6,036,773-9,271,860 LOC105373407, LOC107985847, 48 more genes
    nsv7041767inversion1nstd229human GRCh38 chr2: 7,061,548-10,183,852 , GRCh37.p13 chr2: 7,201,679-10,323,978 LINC00298, KLF11, 52 more genes
    nsv6675178copy number variation1nstd229human GRCh38 chr2: 9,002,054-9,002,095 , GRCh37.p13 chr2: 9,142,183-9,142,224 MBOAT2
    nsv6674137copy number variation1nstd229human GRCh38 chr2: 8,932,486-8,939,718 , GRCh37.p13 chr2: 9,072,615-9,079,847 MBOAT2
    nsv6671544copy number variation1nstd229human GRCh38 chr2: 8,983,408-8,983,523 , GRCh37.p13 chr2: 9,123,537-9,123,652 MBOAT2
    nsv6670111copy number variation1nstd229human GRCh38 chr2: 8,965,365-8,967,646 , GRCh37.p13 chr2: 9,105,494-9,107,775 MBOAT2
    nsv6669809copy number variation1nstd229human GRCh38 chr2: 8,965,361-8,965,773 , GRCh37.p13 chr2: 9,105,490-9,105,902 MBOAT2
    nsv6666643copy number variation1nstd229human GRCh38 chr2: 8,894,447-8,902,702 , GRCh37.p13 chr2: 9,034,577-9,042,832 MBOAT2
    nsv6666576copy number variation1nstd229human GRCh38 chr2: 6,592,339-11,769,396 , GRCh37.p13 chr2: 6,732,471-11,909,522 RN7SKP112, LOC101929861, 103 more genes
    nsv6666550copy number variation1nstd229human GRCh38 chr2: 8,917,546-8,917,773 , GRCh37.p13 chr2: 9,057,676-9,057,903 MBOAT2
    nsv6665332copy number variation1nstd229human GRCh38 chr2: 8,957,202-9,030,737 , GRCh37.p13 chr2: 9,097,331-9,170,866 HMGB1P25, MBOAT2
    nsv6662978copy number variation1nstd229human GRCh38 chr2: 8,842,587-8,906,912 , GRCh37.p13 chr2: 8,982,717-9,047,042 MBOAT2
    nsv6662113copy number variation1nstd229human GRCh38 chr2: 8,915,915-8,920,527 , GRCh37.p13 chr2: 9,056,045-9,060,657 MBOAT2
    nsv6659378copy number variation1nstd229human GRCh38 chr2: 8,978,647-8,982,085 , GRCh37.p13 chr2: 9,118,776-9,122,214 MBOAT2
    nsv6658151copy number variation1nstd229human GRCh38 chr2: 8,893,597-8,895,606 , GRCh37.p13 chr2: 9,033,727-9,035,736 MBOAT2
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 LOC105374455, RN7SL674P, 504 more genes
    nsv6355213copy number variation1nstd223human GRCh38 chr2: 8,938,538-8,938,663 , GRCh37.p13 chr2: 9,078,667-9,078,792 MBOAT2
    nsv6351352copy number variation1nstd223human GRCh38 chr2: 8,960,349-8,960,759 , GRCh37.p13 chr2: 9,100,478-9,100,888 MBOAT2
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