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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098931copy number variation1nstd102humanPathogenic GRCh38 chr22: 16,804,110-18,162,024 , GRCh37.p13 chr22: 17,285,000-18,644,791 SLC25A18, LINC01634, 44 more genes
    nsv7095928copy number variation2nstd102humanPathogenic GRCh37 chr22: 17,565,982-20,052,185 , GRCh38.p12 chr22: 17,085,092-20,064,662 CA15P1, BID, 103 more genes
    nsv7095815copy number variation1nstd102humanUncertain significance GRCh37 chr22: 17,565,982-18,613,903 , GRCh38.p12 chr22: 17,085,092-18,131,136 HDHD5, LINC01664, 30 more genes
    nsv7037548copy number variation1nstd229human GRCh38 chr22: 17,739,575-17,739,723 , GRCh37.p13 chr22: 18,222,341-18,222,489 BID
    nsv7037352copy number variation1nstd229human GRCh38 chr22: 17,727,361-18,091,837 , GRCh37.p13 chr22: 18,210,127-18,574,603 LOC105372853, BCL2L13, 8 more genes
    nsv7033626copy number variation1nstd229human GRCh38 chr22: 17,712,953-17,735,637 , GRCh37.p13 chr22: 18,195,719-18,218,403 BID, BCL2L13
    nsv7031387copy number variation1nstd229human GRCh38 chr22: 17,747,397-17,757,379 , GRCh37.p13 chr22: 18,230,163-18,240,145 BID
    nsv7026423copy number variation1nstd229human GRCh38 chr22: 17,757,875-17,758,593 , GRCh37.p13 chr22: 18,240,641-18,241,359 BID
    nsv7025515copy number variation1nstd229human GRCh38 chr22: 17,750,701-17,753,400 , GRCh37.p13 chr22: 18,233,467-18,236,166 BID
    nsv7023654copy number variation1nstd229human GRCh38 chr22: 17,737,011-17,738,130 , GRCh37.p13 chr22: 18,219,777-18,220,896 BID
    nsv7021855copy number variation1nstd229human GRCh38 chr22: 17,706,289-17,753,246 , GRCh37.p13 chr22: 18,189,055-18,236,012 BCL2L13, BID
    nsv7019323copy number variation1nstd229human GRCh38 chr22: 17,757,576-17,759,460 , GRCh37.p13 chr22: 18,240,342-18,242,226 BID
    nsv6637923copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,900-18,916,828 , GRCh38.p12 chr22: 16,408,174-18,929,315 ANKRD62P1, IGKV1OR22-1, 87 more genes
    nsv6637447copy number variation1nstd102humanUncertain significance GRCh37 chr22: 17,570,796-19,695,101 , GRCh38.p12 chr22: 17,089,906-19,707,578 FAM230J, RN7SL168P, 88 more genes
    nsv6637374copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,900-18,649,190 , GRCh38.p12 chr22: 16,408,174-18,166,423 KCNMB3P1, CECR7, 59 more genes
    nsv6554164copy number variation1nstd223human GRCh38 chr22: 17,755,568-17,759,064 , GRCh37.p13 chr22: 18,238,334-18,241,830 BID
    nsv6552964copy number variation1nstd223human GRCh38 chr22: 17,747,886-17,748,358 , GRCh37.p13 chr22: 18,230,652-18,231,124 BID
    nsv6552392copy number variation1nstd223human GRCh38 chr22: 17,750,637-17,751,241 , GRCh37.p13 chr22: 18,233,403-18,234,007 BID
    nsv6551573copy number variation1nstd223human GRCh38 chr22: 17,759,076-17,760,082 , GRCh37.p13 chr22: 18,241,842-18,242,848 BID
    nsv6550214copy number variation1nstd223human GRCh38 chr22: 17,745,901-17,748,358 , GRCh37.p13 chr22: 18,228,667-18,231,124 BID
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