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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3116050copy number variation42nstd145human GRCh37 chr14: 41,610,263-41,668,279 , GRCh38.p12 chr14: 41,141,060-41,199,076 LINC02315
    nsv3117064copy number variation1nstd145human GRCh37 chr1: 185,291,706-185,321,076 , GRCh38.p12 chr1: 185,322,574-185,351,944 GS1-279B7.1
    nsv3116994copy number variation25nstd145human GRCh37 chr16: 55,799,053-55,821,304 , GRCh38.p12 chr16: 55,765,141-55,787,392 CES1P1
    nsv3114280copy number variation1nstd145human GRCh37 chr14: 48,068,213-48,085,471 , GRCh38.p12 chr14: 47,599,010-47,616,268 MDGA2
    nsv3114057copy number variation160nstd145human GRCh37 chr19: 52,134,789-52,148,550 , GRCh38.p12 chr19: 51,631,536-51,645,297 SIGLEC14
    nsv3111509copy number variation29nstd145human GRCh37 chr8: 2,150,517-2,161,441 , GRCh38.p12 chr8|NT_187576.1: 385,727-396,651 , GRCh38.p12 chr8: 2,202,878-2,213,774 LOC105377782
    nsv3116740copy number variation11nstd145human GRCh37 chr1: 213,002,706-213,013,189 , GRCh38.p12 chr1: 212,829,364-212,839,847 SPATA45
    nsv3110942copy number variation60nstd145human GRCh37 chr7: 91,033,585-91,042,496 , GRCh38.p12 chr7: 91,404,270-91,413,181 LINC02932
    nsv3112146copy number variation37nstd145human GRCh37 chr11: 93,695,236-93,701,577 , GRCh38.p12 chr11: 93,962,070-93,968,411 LOC101060084
    nsv3115994copy number variation2nstd145human GRCh37 chr13: 79,203,351-79,209,249 , GRCh38.p12 chr13: 78,629,216-78,635,114 OBI1
    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
    nsv3114401copy number variation17nstd145human GRCh37 chr7: 89,520,337-89,525,616 , GRCh38.p12 chr7: 89,891,023-89,896,302 STEAP2-AS1
    nsv3115834copy number variation9nstd145human GRCh37 chr1: 234,703,554-234,708,731 , GRCh38.p12 chr1: 234,567,808-234,572,985 LOC107985465
    nsv3116148copy number variation97nstd145human GRCh37 chr8: 594,429-599,002 , GRCh38.p12 chr8: 644,429-649,002 ERICH1
    nsv3113825copy number variation1nstd145human GRCh37 chr13: 78,954,382-78,958,256 , GRCh38.p12 chr13: 78,380,247-78,384,121 OBI1-AS1
    nsv3116722copy number variation1nstd145human GRCh37 chr4: 107,056,600-107,060,161 , GRCh38.p12 chr4: 106,135,443-106,139,004 TBCK
    nsv3117603copy number variation25nstd145human GRCh37 chr9: 28,047,569-28,050,923 , GRCh38.p12 chr9: 28,047,571-28,050,925 LINGO2
    nsv3118304copy number variation1nstd145human GRCh37 chr19: 54,557,372-54,560,055 , GRCh38.p12 chr19|NW_003571061.2: 28,485-31,168 , GRCh38.p12 chr19|NW_003571057.2: 28,485-31,168 , GRCh38.p12 chr19|NW_003571058.2: 28,485-31,168 , GRCh38.p12 chr19|NW_003571059.2: 28,485-31,168 , GRCh38.p12 chr19|NW_003571060.1: 28,485-31,168 , GRCh38.p12 chr19|NW_003571056.2: 28,485-31,168 , GRCh38.p12 chr19|NW_003571055.2: 28,485-31,168 , GRCh38.p12 chr19|NW_003571054.1: 28,485-31,168 , GRCh38.p12 chr19: 54,054,118-54,056,801 , GRCh38.p12 chr19|NT_187693.1: 28,485-31,168 VSTM1
    nsv3111699copy number variation11nstd145human GRCh37 chr6: 133,954,760-133,956,912 , GRCh38.p12 chr6: 133,633,622-133,635,774 TARID
    nsv3114313copy number variation35nstd145human GRCh37 chr12: 74,644,721-74,646,871 , GRCh38.p12 chr12: 74,250,941-74,253,091 LINC02882
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