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Items: 1 to 20 of 448

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6127870copy number variation1nstd186human GRCh37 chr22: 50,949,780-50,950,136 , GRCh38.p12 chr22: 50,511,351-50,511,707 NCAPH2
    nsv6112794copy number variation1nstd102humanPathogenic GRCh37 chr22: 50,099,570-51,187,115 , GRCh38.p12 chr22: 49,705,922-50,748,687 SCO2, CIMAP1B, 50 more genes
    nsv5964136copy number variation1nstd209human GRCh38 chr22: 50,511,351-50,511,706 , GRCh37.p13 chr22: 50,949,780-50,950,135 NCAPH2
    nsv5958830copy number variation1nstd209human GRCh38 chr22: 50,521,319-50,521,383 , GRCh37.p13 chr22: 50,959,748-50,959,812 NCAPH2
    nsv5958181copy number variation1nstd209human GRCh38 chr22: 50,511,101-50,511,545 , GRCh37.p13 chr22: 50,949,530-50,949,974 NCAPH2
    nsv5673438copy number variation1nstd102humanPathogenic GRCh37 chr22: 50,297,466-51,066,227 , GRCh38.p12 chr22: 49,903,818-50,627,799 MIR6821, CHKB, 39 more genes
    nsv5600465copy number variation1nstd207human GRCh38 chr22: 50,511,351-50,511,706 , GRCh37.p13 chr22: 50,949,780-50,950,135 NCAPH2
    nsv5595504copy number variation1nstd207human GRCh38 chr22: 50,521,319-50,521,383 , GRCh37.p13 chr22: 50,959,748-50,959,812 NCAPH2
    nsv5591905copy number variation1nstd207human GRCh38 chr22: 50,507,735-50,507,824 , GRCh37.p13 chr22: 50,946,164-50,946,253 LMF2, NCAPH2
    nsv5392608copy number variation1nstd186human GRCh37 chr22: 50,949,668-50,950,121 , GRCh38.p12 chr22: 50,511,239-50,511,692 NCAPH2
    nsv5392156copy number variation1nstd186human GRCh37 chr22: 50,949,735-50,950,114 , GRCh38.p12 chr22: 50,511,306-50,511,685 NCAPH2
    nsv5381149copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,333,802-51,195,728 , GRCh38.p12 chr22: 41,937,798-50,757,300 WBP2NL, RN7SKP80, 210 more genes
    nsv5283635copy number variation1nstd204human GRCh38.p13 chr22: 50,181,501-50,588,000 , GRCh37.p13 chr22: 50,619,930-51,026,429 , SYCE3, 29 more genes
    nsv5281266copy number variation1nstd204human GRCh38.p13 chr22: 50,508,101-50,600,500 , GRCh37.p13 chr22: 50,946,530-51,038,929 NCAPH2, CHKB, 13 more genes
    nsv5036107copy number variation1nstd200human GRCh38 chr22: 50,486,769-50,596,549 , GRCh37.p13 chr22: 50,925,198-51,034,978 KLHDC7B-DT, CPT1B, 14 more genes
    nsv5035208copy number variation1nstd200human GRCh38 chr22: 48,120,092-50,757,227 , GRCh37.p13 chr22: 48,515,909-51,195,655 , CRELD2, 70 more genes
    nsv5030782copy number variation1nstd200human GRCh38 chr22: 50,505,488-50,525,223 , GRCh37.p13 chr22: 50,943,917-50,963,652 SCO2, NCAPH2, 2 more genes
    nsv5030619copy number variation1nstd200human GRCh38 chr22: 49,877,723-50,553,750 , GRCh37.p13 chr22: 50,271,371-50,992,179 , TUBGCP6, 35 more genes
    nsv5029873copy number variation1nstd200human GRCh38 chr22: 50,511,238-50,511,692 , GRCh37.p13 chr22: 50,949,667-50,950,121 NCAPH2
    nsv5029581copy number variation1nstd200human GRCh38 chr22: 50,511,932-50,515,629 , GRCh37.p13 chr22: 50,950,361-50,954,058 NCAPH2
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