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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
    nsv3117875copy number variation1nstd145human GRCh37 chr2: 33,955,538-33,980,346 , GRCh38.p12 chr2: 33,730,471-33,755,279 LINC01317
    nsv3114943copy number variation13nstd145human GRCh37 chr14: 86,547,386-86,570,395 , GRCh38.p12 chr14: 86,081,042-86,104,051 LINC02328
    nsv3117809copy number variation152nstd145human GRCh37 chr20: 1,561,593-1,584,273 , GRCh38.p12 chr20: 1,580,947-1,603,627 SIRPB1
    nsv3114769copy number variation2nstd145human GRCh37 chr3: 88,469,273-88,479,733 , GRCh38.p12 chr3: 88,420,123-88,430,583 CSNKA2IP
    nsv3118025copy number variation35nstd145human GRCh37 chr8: 15,402,271-15,412,465 , GRCh38.p12 chr8: 15,544,762-15,554,956 TUSC3
    nsv3113383copy number variation199nstd145human GRCh37 chr3: 192,875,554-192,885,008 , GRCh38.p12 chr3: 193,157,765-193,167,219 VEZF1P1
    nsv3110725copy number variation5nstd145human GRCh37 chr10: 69,327,392-69,335,804 , GRCh38.p12 chr10: 67,567,634-67,576,046 CTNNA3
    nsv3117708copy number variation1nstd145human GRCh37 chr2: 49,531,903-49,538,521 , GRCh38.p12 chr2: 49,304,764-49,311,382 LOC105374595
    nsv3112895copy number variation76nstd145human GRCh37 chr12: 43,020,941-43,027,293 , GRCh38.p12 chr12: 42,627,139-42,633,491 LINC02402
    nsv3112146copy number variation37nstd145human GRCh37 chr11: 93,695,236-93,701,577 , GRCh38.p12 chr11: 93,962,070-93,968,411 LOC101060084
    nsv3113862copy number variation4nstd145human GRCh37 chr3: 189,365,003-189,370,847 , GRCh38.p12 chr3: 189,647,214-189,653,058 TP63
    nsv3117110copy number variation7nstd145human GRCh37 chr8: 87,188,232-87,193,436 , GRCh38.p12 chr8: 86,176,003-86,181,207 LOC105375623
    nsv3113836copy number variation16nstd145human GRCh37 chr4: 53,338,728-53,343,913 , GRCh38.p12 chr4: 52,472,562-52,477,747
    nsv3111075copy number variation9nstd145human GRCh37 chr7: 154,392,836-154,397,841 , GRCh38.p12 chr7: 154,601,126-154,606,131 DPP6
    nsv3113205copy number variation26nstd145human GRCh37 chr3: 131,708,215-131,712,626 , GRCh38.p12 chr3: 131,989,371-131,993,782 CPNE4
    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
    nsv3113114copy number variation2nstd145human GRCh37 chr12: 82,139,806-82,143,711 , GRCh38.p12 chr12: 81,746,027-81,749,932 PPFIA2
    nsv3114524copy number variation6nstd145human GRCh37 chr8: 594,429-598,086 , GRCh38.p12 chr8: 644,429-648,086 ERICH1
    nsv3115565copy number variation1nstd145human GRCh37 chr7: 91,038,006-91,041,387 , GRCh38.p12 chr7: 91,408,691-91,412,072 LINC02932
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