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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3116114copy number variation4nstd145human GRCh37 chr9: 11,734,260-12,069,616 , GRCh38.p12 chr9: 11,734,260-12,069,616 LOC101929446
    nsv3111002copy number variation2nstd145human GRCh37 chr13: 58,709,445-58,765,525 , GRCh38.p12 chr13: 58,135,311-58,191,391 LINC02338
    nsv3117354copy number variation83nstd145human GRCh37 chr17: 15,043,995-15,058,468 , GRCh38.p12 chr17: 15,140,678-15,155,151 LOC107984976
    nsv3114057copy number variation160nstd145human GRCh37 chr19: 52,134,789-52,148,550 , GRCh38.p12 chr19: 51,631,536-51,645,297 SIGLEC14
    nsv3111250copy number variation1nstd145human GRCh37 chr11: 55,445,882-55,459,554 , GRCh38.p12 chr11: 55,678,406-55,692,078 OR4P1P
    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
    nsv3114521copy number variation39nstd145human GRCh37 chr18: 66,745,828-66,756,183 , GRCh38.p12 chr18: 69,078,591-69,088,946 CCDC102B
    nsv3117329copy number variation1nstd145human GRCh37 chr2: 43,738,275-43,747,979 , GRCh38.p12 chr2: 43,511,136-43,520,840 THADA
    nsv3113383copy number variation199nstd145human GRCh37 chr3: 192,875,554-192,885,008 , GRCh38.p12 chr3: 193,157,765-193,167,219 VEZF1P1
    nsv3115066copy number variation81nstd145human GRCh37 chr6: 19,042,250-19,049,222 , GRCh38.p12 chr6: 19,042,019-19,048,991 LOC105374958
    nsv3118086copy number variation1nstd145human GRCh37 chr15: 29,898,981-29,905,835 , GRCh38.p12 chr15: 29,606,777-29,613,631 , GRCh38.p12 chr15|NT_187660.1: 1,890,892-1,897,752 , GRCh38.p12 chr15|NW_011332701.1: 1,778,408-1,785,268 TUBBP8
    nsv3112895copy number variation76nstd145human GRCh37 chr12: 43,020,941-43,027,293 , GRCh38.p12 chr12: 42,627,139-42,633,491 LINC02402
    nsv3113584copy number variation4nstd145human GRCh37 chr12: 82,139,386-82,144,215 , GRCh38.p12 chr12: 81,745,607-81,750,436 PPFIA2
    nsv3113172copy number variation17nstd145human GRCh37 chr7: 112,515,072-112,519,782 , GRCh38.p12 chr7: 112,875,017-112,879,727 BMT2
    nsv3117774copy number variation53nstd145human GRCh37 chr1: 174,796,674-174,801,029 , GRCh38.p12 chr1: 174,827,536-174,831,891 RABGAP1L
    nsv3117206copy number variation28nstd145human GRCh37 chr4: 138,095,710-138,099,949 , GRCh38.p12 chr4: 137,174,556-137,178,795 LINC02511
    nsv3113333copy number variation2nstd145human GRCh37 chrX: 148,711,463-148,714,830 , GRCh38.p12 chrX: 149,629,782-149,633,174 TMEM185A
    nsv3112142copy number variation5nstd145human GRCh37 chr1: 42,685,879-42,689,215 , GRCh38.p12 chr1: 42,220,208-42,223,544 FOXJ3
    nsv3113339copy number variation34nstd145human GRCh37 chr3: 189,737,484-189,740,185 , GRCh38.p12 chr3: 190,019,695-190,022,396 P3H2
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