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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3116114copy number variation4nstd145human GRCh37 chr9: 11,734,260-12,069,616 , GRCh38.p12 chr9: 11,734,260-12,069,616 LOC101929446
    nsv3115682copy number variation2nstd145human GRCh37 chr11: 49,712,397-49,754,911 , GRCh38.p12 chr11: 49,690,845-49,733,359 , GRCh38.p12 chr11|NW_019805495.1: 154,979-197,508 GRM5P1
    nsv3115237copy number variation7nstd145human GRCh37 chr1: 169,216,111-169,240,805 , GRCh38.p12 chr1: 169,246,873-169,271,567 NME7
    nsv3117809copy number variation152nstd145human GRCh37 chr20: 1,561,593-1,584,273 , GRCh38.p12 chr20: 1,580,947-1,603,627 SIRPB1
    nsv3110960copy number variation10nstd145human GRCh37 chr4: 69,435,444-69,456,801 , GRCh38.p12 chr4: 68,569,726-68,591,083 UGT2B17
    nsv3113108copy number variation1nstd145human GRCh37 chr4: 107,521,310-107,540,212 , GRCh38.p12 chr4: 106,600,153-106,619,055 LOC105377356
    nsv3116740copy number variation11nstd145human GRCh37 chr1: 213,002,706-213,013,189 , GRCh38.p12 chr1: 212,829,364-212,839,847 SPATA45
    nsv3110757copy number variation1nstd145human GRCh37 chr22: 40,868,225-40,878,592 , GRCh38.p12 chr22: 40,472,221-40,482,588 MRTFA
    nsv3114938copy number variation3nstd145human GRCh37 chr1: 231,535,550-231,545,858 , GRCh38.p12 chr1: 231,399,804-231,410,112 EGLN1
    nsv3114126copy number variation1nstd145human GRCh37 chr7: 151,591,171-151,599,330 , GRCh38.p12 chr7: 151,894,086-151,902,245 RNU6-604P
    nsv3116750copy number variation1nstd145human GRCh37 chr9: 26,713,313-26,719,612 , GRCh38.p12 chr9: 26,713,315-26,719,614 LOC105376000
    nsv3112869copy number variation2nstd145human GRCh37 chr3: 195,137,195-195,142,873 , GRCh38.p12 chr3: 195,416,466-195,422,144 ACAP2
    nsv3115834copy number variation9nstd145human GRCh37 chr1: 234,703,554-234,708,731 , GRCh38.p12 chr1: 234,567,808-234,572,985 LOC107985465
    nsv3117813copy number variation1nstd145human GRCh37 chr15: 32,510,485-32,514,993 , GRCh38.p12 chr15: 32,218,284-32,222,792 LOC102724078
    nsv3112302copy number variation5nstd145human GRCh37 chr3: 192,875,554-192,880,029 , GRCh38.p12 chr3: 193,157,765-193,162,240 VEZF1P1
    nsv3113906copy number variation2nstd145human GRCh37 chr3: 22,281,309-22,285,481 , GRCh38.p12 chr3: 22,239,817-22,243,989 ZNF385D
    nsv3111918copy number variation6nstd145human GRCh37 chrX: 112,161,399-112,165,353 , GRCh38.p12 chrX: 112,918,171-112,922,125 RNU6-1015P
    nsv3112247copy number variation2nstd145human GRCh37 chr11: 79,870,834-79,874,111 , GRCh38.p12 chr11: 80,159,790-80,163,067 LOC105369406
    nsv3115311copy number variation23nstd145human GRCh37 chr3: 189,737,302-189,740,185 , GRCh38.p12 chr3: 190,019,513-190,022,396 P3H2
    nsv3117776copy number variation27nstd145human GRCh37 chr9: 20,801,780-20,804,551 , GRCh38.p12 chr9: 20,801,781-20,804,552 FOCAD
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