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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3110127copy number variation4nstd145human GRCh37 chr16: 55,799,089-55,821,304 , GRCh38.p12 chr16: 55,765,177-55,787,392 CES1P1
    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
    nsv3111623copy number variation16nstd145human GRCh37 chr5: 41,232,035-41,243,881 , GRCh38.p12 chr5: 41,231,933-41,243,779 C6
    nsv3114521copy number variation39nstd145human GRCh37 chr18: 66,745,828-66,756,183 , GRCh38.p12 chr18: 69,078,591-69,088,946 CCDC102B
    nsv3111854copy number variation1nstd145human GRCh37 chr5: 107,363,611-107,373,064 , GRCh38.p12 chr5: 108,027,910-108,037,363 FBXL17
    nsv3113944copy number variation1nstd145human GRCh37 chr11: 27,564,158-27,573,115 , GRCh38.p12 chr11: 27,542,611-27,551,568 BDNF-AS
    nsv3112839copy number variation1nstd145human GRCh37 chr2: 162,681,875-162,690,281 , GRCh38.p12 chr2: 161,825,365-161,833,771 SLC4A10
    nsv3115104copy number variation1nstd145human GRCh37 chr14: 22,831,961-22,840,093 , GRCh38.p12 chr14: 22,363,534-22,371,688 TRA
    nsv3117209copy number variation1nstd145human GRCh37 chr11: 5,120,715-5,128,364 , GRCh38.p12 chr11: 5,099,485-5,107,134 OR52J1P
    nsv3114475copy number variation50nstd145human GRCh37 chr5: 12,811,448-12,818,768 , GRCh38.p12 chr5: 12,811,336-12,818,656 LOC105374657
    nsv3112146copy number variation37nstd145human GRCh37 chr11: 93,695,236-93,701,577 , GRCh38.p12 chr11: 93,962,070-93,968,411 LOC101060084
    nsv3112036copy number variation2nstd145human GRCh37 chr7: 151,626-157,474 , GRCh38.p12 chr7: 151,626-157,474 , GRCh38.p12 chr7|NT_187558.1: 107,431-113,280 , GRCh38.p12 chr7|NT_187653.1: 143,947-149,795 LINC03014
    nsv3112488copy number variation14nstd145human GRCh37 chr7: 16,794,950-16,800,421 , GRCh38.p12 chr7: 16,755,325-16,760,796 TSPAN13
    nsv3116468copy number variation1nstd145human GRCh37 chr6: 169,463,891-169,469,261 , GRCh38.p12 chr6: 169,063,796-169,069,166 LOC102724357
    nsv3118302copy number variation1nstd145human GRCh37 chr3: 150,820,691-150,825,807 , GRCh38.p12 chr3: 151,102,904-151,108,020 MED12L
    nsv3111075copy number variation9nstd145human GRCh37 chr7: 154,392,836-154,397,841 , GRCh38.p12 chr7: 154,601,126-154,606,131 DPP6
    nsv3115871copy number variation21nstd145human GRCh37 chr11: 99,647,381-99,652,155 , GRCh38.p12 chr11: 99,776,650-99,781,424 CNTN5
    nsv3118171copy number variation2nstd145human GRCh37 chr16: 83,532,108-83,536,771 , GRCh38.p12 chr16: 83,498,503-83,503,166 CDH13
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