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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    nsv1112539copy number variation1nstd106human GRCh37 chr1: 103,785,200-103,913,900 , GRCh38.p12 chr1: 103,382,377-103,461,016 RNPC3-DT
    nsv1112540copy number variation1nstd106human GRCh37 chr1: 103,925,200-104,003,800 , GRCh38.p12 chr1: 103,382,578-103,461,178 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
    nsv1121944copy number variation2nstd106human GRCh37 chr17: 79,709,000-79,759,100 , GRCh38.p12 chr17: 81,741,970-81,801,224 LOC105376789
    nsv1121886copy number variation1nstd106human GRCh37 chr15: 20,880,400-20,935,100 , GRCh38.p12 chr15: 20,675,071-20,729,771 NBEAP1
    nsv1137592copy number variation1nstd106human GRCh37 chr7: 143,347,700-143,401,100 , GRCh38.p12 chr7: 143,650,607-143,704,007 TCAF2
    nsv1133764copy number variation1nstd106human GRCh37 chrX: 52,102,500-52,154,500 , GRCh38.p12 chrX: 52,359,357-52,411,357 XAGE2
    nsv1112235copy number variation1nstd106human GRCh37 chr10: 53,984,266-54,033,935 , GRCh38.p12 chr10: 52,224,506-52,274,175 PRKG1
    nsv1112852copy number variation1nstd106human GRCh37 chr4: 34,780,100-34,829,000 , GRCh38.p12 chr4: 34,778,478-34,827,378 , GRCh38.p12 chr4|NW_003315915.1: 270,807-319,707 LOC105378262
    nsv1133727copy number variation1nstd106human GRCh37 chr9: 66,123,600-66,170,200 , GRCh38.p12 chr9: 66,786,194-66,832,794 CNTNAP3P9
    nsv1133731copy number variation1nstd106human GRCh37 chr9: 67,544,100-67,587,800 , GRCh38.p12 chr9: 62,068,356-62,112,056 LOC107987008
    nsv1112814copy number variation1nstd106human GRCh37 chr22: 25,410,900-25,454,600 , GRCh38.p12 chr22: 25,014,933-25,058,633 KIAA1671
    nsv1133586copy number variation1nstd106human GRCh37 chr4: 75,281,300-75,323,200 , GRCh38.p12 chr4: 74,415,583-74,457,483 AREG
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