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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1126862copy number variation1nstd106human GRCh37 chr8: 142,745,700-142,825,800 , GRCh38.p12 chr8: 141,735,285-141,888,945 MIR1302-7
    nsv1112968copy number variation1nstd106human GRCh37 chr8: 142,763,300-142,826,000 , GRCh38.p12 chr8: 141,735,285-141,888,945 MIR1302-7
    nsv1112587copy number variation1nstd106human GRCh37 chr10: 48,663,400-48,772,500 , GRCh38.p12 chr10: 46,966,862-47,075,962 PTPN20
    nsv1112721copy number variation1nstd106human GRCh37 chr17: 77,546,300-77,630,800 , GRCh38.p12 chr17: 79,550,216-79,656,948 RBFOX3
    nsv1126472copy number variation1nstd106human GRCh37 chr17: 77,546,400-77,630,800 , GRCh38.p12 chr17: 79,550,316-79,656,948 RBFOX3
    nsv1126255copy number variation1nstd106human GRCh37 chr10: 48,663,900-48,757,600 , GRCh38.p12 chr10: 46,981,762-47,075,462 PTPN20
    nsv1111805copy number variation1nstd106human GRCh37 chr2: 51,297,300-51,383,200 , GRCh38.p12 chr2: 51,070,162-51,156,062 NRXN1-DT
    nsv1120749copy number variation1nstd106human GRCh37 chr2: 51,297,277-51,383,153 , GRCh38.p12 chr2: 51,070,139-51,156,015 NRXN1-DT
    nsv1143451copy number variation1nstd106human GRCh37 chr1: 103,785,000-103,913,900 , GRCh38.p12 chr1: 103,382,377-103,461,016 RNPC3-DT
    nsv1112539copy number variation1nstd106human GRCh37 chr1: 103,785,200-103,913,900 , GRCh38.p12 chr1: 103,382,377-103,461,016 RNPC3-DT
    nsv1126835copy number variation1nstd106human GRCh37 chr8: 7,474,500-7,553,100 , GRCh38.p12 chr8: 7,616,978-7,695,578 LOC101929400
    nsv1112540copy number variation1nstd106human GRCh37 chr1: 103,925,200-104,003,800 , GRCh38.p12 chr1: 103,382,578-103,461,178 RNPC3-DT
    nsv1126200copy number variation1nstd106human GRCh37 chr1: 103,925,300-104,003,500 , GRCh38.p12 chr1: 103,382,678-103,460,878 RNPC3-DT
    nsv1130969copy number variation1nstd106human GRCh37 chr1: 146,306,100-146,383,500 , GRCh38.p12 chr1: 146,870,866-146,948,310 NBPF12
    nsv1122263copy number variation2nstd106human GRCh37 chrX: 49,974,100-50,024,200 , GRCh38.p12 chrX: 50,209,449-50,281,200 CCNB3
    nsv1122213copy number variation1nstd106human GRCh37 chr9: 40,869,700-40,990,700 , GRCh38.p12 chr9: 66,752,605-66,823,145 CNTNAP3P9
    nsv1126753copy number variation1nstd106human GRCh37 chr6: 78,967,200-79,036,500 , GRCh38.p12 chr6: 78,257,483-78,326,783 LOC105377865
    nsv1145191copy number variation1nstd106human GRCh37 chr8: 12,087,000-12,150,900 , GRCh38.p12 chr8: 12,229,491-12,293,391 DEFB131D
    nsv1145237copy number variation1nstd106human GRCh37 chr9: 65,524,800-65,584,900 , GRCh38.p12 chr9: 61,114,746-61,174,846 LOC105379249
    nsv1121944copy number variation2nstd106human GRCh37 chr17: 79,709,000-79,759,100 , GRCh38.p12 chr17: 81,741,970-81,801,224 LOC105376789
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