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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3118102copy number variation23nstd145human GRCh37 chr14: 41,610,669-41,668,279 , GRCh38.p12 chr14: 41,141,466-41,199,076 LINC02315
    nsv3114733copy number variation1nstd145human GRCh37 chr10: 68,380,583-68,422,070 , GRCh38.p12 chr10: 66,620,825-66,662,312 CTNNA3
    nsv3112298copy number variation1nstd145human GRCh37 chr1: 197,231,212-197,254,680 , GRCh38.p12 chr1: 197,262,082-197,285,550 CRB1
    nsv3112646copy number variation3nstd145human GRCh37 chr5: 113,950,043-113,973,417 , GRCh38.p12 chr5: 114,614,346-114,637,720 LOC101927078
    nsv3117809copy number variation152nstd145human GRCh37 chr20: 1,561,593-1,584,273 , GRCh38.p12 chr20: 1,580,947-1,603,627 SIRPB1
    nsv3117855copy number variation14nstd145human GRCh37 chr19: 41,351,463-41,372,509 , GRCh38.p12 chr19: 40,845,558-40,866,604 CYP2A6
    nsv3117354copy number variation83nstd145human GRCh37 chr17: 15,043,995-15,058,468 , GRCh38.p12 chr17: 15,140,678-15,155,151 LOC107984976
    nsv3111733copy number variation53nstd145human GRCh37 chr1: 169,227,837-169,240,805 , GRCh38.p12 chr1: 169,258,599-169,271,567 NME7
    nsv3112094copy number variation94nstd145human GRCh37 chr7: 133,785,285-133,797,218 , GRCh38.p12 chr7: 134,100,532-134,112,465
    nsv3110986copy number variation37nstd145human GRCh37 chr5: 17,640,200-17,651,341 , GRCh38.p12 chr5: 17,640,091-17,651,232 LOC391768
    nsv3117380copy number variation44nstd145human GRCh37 chr21: 23,655,218-23,665,891 , GRCh38.p12 chr21: 22,282,898-22,293,571 , GRCh38.p12 chr21|NW_003315968.2: 187,127-197,800 LOC107985508
    nsv3113383copy number variation199nstd145human GRCh37 chr3: 192,875,554-192,885,008 , GRCh38.p12 chr3: 193,157,765-193,167,219 VEZF1P1
    nsv3116140copy number variation45nstd145human GRCh37 chr4: 21,369,066-21,376,838 , GRCh38.p12 chr4: 21,367,443-21,375,215 KCNIP4
    nsv3117894copy number variation2nstd145human GRCh37 chr12: 86,695,674-86,702,865 , GRCh38.p12 chr12: 86,301,896-86,309,087 MGAT4C
    nsv3117297copy number variation80nstd145human GRCh37 chr7: 154,392,836-154,399,317 , GRCh38.p12 chr7: 154,601,126-154,607,607 DPP6
    nsv3115158copy number variation1nstd145human GRCh37 chr18: 1,307,241-1,313,535 , GRCh38.p12 chr18: 1,307,240-1,313,534 LINC00470
    nsv3114178copy number variation107nstd145human GRCh37 chr6: 53,928,991-53,933,879 , GRCh38.p12 chr6: 54,064,193-54,069,081 MLIP
    nsv3115269copy number variation5nstd145human GRCh37 chr3: 2,569,789-2,574,660 , GRCh38.p12 chr3: 2,528,105-2,532,976 CNTN4
    nsv3115871copy number variation21nstd145human GRCh37 chr11: 99,647,381-99,652,155 , GRCh38.p12 chr11: 99,776,650-99,781,424 CNTN5
    nsv3113139copy number variation39nstd145human GRCh37 chr13: 32,533,792-32,538,481 , GRCh38.p12 chr13: 31,959,655-31,964,344 EEF1DP3
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