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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3117955copy number variation13nstd145human GRCh37 chr19: 41,351,463-41,379,048 , GRCh38.p12 chr19: 40,845,558-40,873,143 CYP2A6
    nsv3117809copy number variation152nstd145human GRCh37 chr20: 1,561,593-1,584,273 , GRCh38.p12 chr20: 1,580,947-1,603,627 SIRPB1
    nsv3116994copy number variation25nstd145human GRCh37 chr16: 55,799,053-55,821,304 , GRCh38.p12 chr16: 55,765,141-55,787,392 CES1P1
    nsv3110854copy number variation4nstd145human GRCh37 chr7: 91,030,673-91,042,496 , GRCh38.p12 chr7: 91,401,358-91,413,181 LINC02932
    nsv3113383copy number variation199nstd145human GRCh37 chr3: 192,875,554-192,885,008 , GRCh38.p12 chr3: 193,157,765-193,167,219 VEZF1P1
    nsv3117920copy number variation33nstd145human GRCh37 chr17: 50,117,130-50,126,228 , GRCh38.p12 chr17: 52,039,770-52,048,868 CA10
    nsv3115066copy number variation81nstd145human GRCh37 chr6: 19,042,250-19,049,222 , GRCh38.p12 chr6: 19,042,019-19,048,991 LOC105374958
    nsv3116197copy number variation63nstd145human GRCh37 chr7: 151,606-157,474 , GRCh38.p12 chr7: 151,606-157,474 , GRCh38.p12 chr7|NT_187558.1: 107,411-113,280 , GRCh38.p12 chr7|NT_187653.1: 143,927-149,795 LINC03014
    nsv3112349copy number variation62nstd145human GRCh37 chr4: 107,056,600-107,062,092 , GRCh38.p12 chr4: 106,135,443-106,140,935 TBCK
    nsv3110401copy number variation14nstd145human GRCh37 chr5: 11,129,609-11,134,869 , GRCh38.p12 chr5: 11,129,497-11,134,757 CTNND2
    nsv3110559copy number variation79nstd145human GRCh37 chr2: 49,534,030-49,539,079 , GRCh38.p12 chr2: 49,306,891-49,311,940 LOC105374595
    nsv3114178copy number variation107nstd145human GRCh37 chr6: 53,928,991-53,933,879 , GRCh38.p12 chr6: 54,064,193-54,069,081 MLIP
    nsv3111869copy number variation2nstd145human GRCh37 chrX: 112,160,689-112,165,353 , GRCh38.p12 chrX: 112,917,461-112,922,125 RNU6-1015P
    nsv3116148copy number variation97nstd145human GRCh37 chr8: 594,429-599,002 , GRCh38.p12 chr8: 644,429-649,002 ERICH1
    nsv3114683copy number variation27nstd145human GRCh37 chr4: 138,095,710-138,099,941 , GRCh38.p12 chr4: 137,174,556-137,178,787 LINC02511
    nsv3111612copy number variation21nstd145human GRCh37 chr8: 3,786,042-3,790,180 , GRCh38.p12 chr8: 3,928,520-3,932,658 CSMD1
    nsv3112046copy number variation55nstd145human GRCh37 chr19: 54,556,015-54,560,055 , GRCh38.p12 chr19: 54,052,761-54,056,801 , GRCh38.p12 chr19|NT_187693.1: 27,128-31,168 , GRCh38.p12 chr19|NW_003571061.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571057.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571058.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571059.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571060.1: 27,128-31,168 , GRCh38.p12 chr19|NW_003571056.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571055.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571054.1: 27,128-31,168 VSTM1
    nsv3116946copy number variation16nstd145human GRCh37 chr1: 106,018,393-106,022,354 , GRCh38.p12 chr1: 105,475,771-105,479,732 LOC105378881
    nsv3117933copy number variation2nstd145human GRCh37 chr1: 74,347,609-74,351,332 , GRCh38.p12 chr1: 73,881,926-73,885,649 RNU4ATAC8P
    nsv3114451copy number variation90nstd145human GRCh37 chr12: 90,487,994-90,491,654 , GRCh38.p12 chr12: 90,094,217-90,097,877 LOC105369890
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