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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3116390copy number variation1nstd145human GRCh37 chr8: 39,335,536-39,385,494 , GRCh38.p12 chr8: 39,478,017-39,527,975 ADAM3A
    nsv3116038copy number variation1nstd145human GRCh37 chr4: 69,431,023-69,458,710 , GRCh38.p12 chr4: 68,565,305-68,592,992 UGT2B17
    nsv3113269copy number variation34nstd145human GRCh37 chr20: 1,558,341-1,584,273 , GRCh38.p12 chr20: 1,577,695-1,603,627 SIRPB1
    nsv3113277copy number variation33nstd145human GRCh37 chr16: 55,797,365-55,821,304 , GRCh38.p12 chr16: 55,763,453-55,787,392 CES1P1
    nsv3117510copy number variation1nstd145human GRCh37 chr1: 169,228,193-169,240,805 , GRCh38.p12 chr1: 169,258,955-169,271,567 NME7
    nsv3110152copy number variation1nstd145human GRCh37 chr21: 41,941,321-41,951,446 , GRCh38.p12 chr21: 40,569,394-40,579,519 DSCAM
    nsv3115066copy number variation81nstd145human GRCh37 chr6: 19,042,250-19,049,222 , GRCh38.p12 chr6: 19,042,019-19,048,991 LOC105374958
    nsv3114208copy number variation43nstd145human GRCh37 chr3: 189,364,561-189,370,847 , GRCh38.p12 chr3: 189,646,772-189,653,058 TP63
    nsv3111576copy number variation2nstd145human GRCh37 chr11: 5,784,834-5,790,776 , GRCh38.p12 chr11: 5,763,604-5,769,546 OR56B2P
    nsv3112371copy number variation15nstd145human GRCh37 chr6: 81,287,765-81,292,398 , GRCh38.p12 chr6: 80,578,048-80,582,681 LOC112267962
    nsv3110593copy number variation88nstd145human GRCh37 chr8: 40,774,871-40,779,295 , GRCh38.p12 chr8: 40,917,352-40,921,776 LOC105379389
    nsv3117571copy number variation81nstd145human GRCh37 chr11: 107,239,191-107,242,941 , GRCh38.p12 chr11: 107,368,465-107,372,215 CWF19L2
    nsv3110984copy number variation1nstd145human GRCh37 chr3: 153,293,398-153,297,094 , GRCh38.p12 chr3: 153,575,609-153,579,305 LINC02006
    nsv3111396copy number variation4nstd145human GRCh37 chr9: 28,047,569-28,050,661 , GRCh38.p12 chr9: 28,047,571-28,050,663 LINGO2
    nsv3111468copy number variation114nstd145human GRCh37 chr2: 33,224,481-33,227,121 , GRCh38.p12 chr2: 32,999,414-33,002,054 LTBP1
    nsv3112729copy number variation26nstd145human GRCh37 chr22: 37,144,518-37,146,950 , GRCh38.p12 chr22: 36,748,474-36,750,906 CACNG2-DT
    nsv3114312copy number variation223nstd145human GRCh37 chr2: 76,773,866-76,775,310 , GRCh38.p12 chr2: 76,546,740-76,548,184 LOC105374814
    nsv3115672copy number variation1nstd145human GRCh37 chr1: 62,113,992-62,115,318 , GRCh38.p12 chr1: 61,648,320-61,649,646 LOC107984964
    nsv3111987copy number variation1nstd145human GRCh37 chr11: 20,847,788-20,849,038 , GRCh38.p12 chr11: 20,826,242-20,827,492 NELL1
    nsv3115989copy number variation1nstd145human GRCh37 chr22: 24,275,601-24,276,189 , GRCh38.p12 chr22: 23,933,414-23,934,002 , GRCh38.p12 chr22|NT_187633.1: 169,776-170,364 LOC100652871
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