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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3110971copy number variation6nstd145human GRCh37 chr11: 97,820,128-97,876,272 , GRCh38.p12 chr11: 97,949,128-98,005,544 LINC02713
    nsv3112482copy number variation23nstd145human GRCh37 chr4: 34,781,013-34,826,967 , GRCh38.p12 chr4: 34,779,391-34,825,345 , GRCh38.p12 chr4|NW_003315915.1: 271,720-317,674 LOC105378262
    nsv3110798copy number variation1nstd145human GRCh37 chr3: 41,542,480-41,580,937 , GRCh38.p12 chr3: 41,500,989-41,539,446 ULK4
    nsv3118081copy number variation72nstd145human GRCh37 chr7: 141,766,533-141,793,377 , GRCh38.p12 chr7|NT_187562.1: 28,613-55,457 , GRCh38.p12 chr7: 142,066,733-142,093,577 MGAM
    nsv3116159copy number variation2nstd145human GRCh37 chr1: 72,798,207-72,812,182 , GRCh38.p12 chr1: 72,332,524-72,346,499 , GRCh38.p12 chr1|NW_018654707.1: 44,791-67,724 LOC105378797
    nsv3110383copy number variation1nstd145human GRCh37 chr1: 178,114,017-178,128,489 , GRCh38.p12 chr1: 178,144,882-178,159,354 RASAL2
    nsv3112094copy number variation94nstd145human GRCh37 chr7: 133,785,285-133,797,218 , GRCh38.p12 chr7: 134,100,532-134,112,465
    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
    nsv3117380copy number variation44nstd145human GRCh37 chr21: 23,655,218-23,665,891 , GRCh38.p12 chr21: 22,282,898-22,293,571 , GRCh38.p12 chr21|NW_003315968.2: 187,127-197,800 LOC107985508
    nsv3113383copy number variation199nstd145human GRCh37 chr3: 192,875,554-192,885,008 , GRCh38.p12 chr3: 193,157,765-193,167,219 VEZF1P1
    nsv3110942copy number variation60nstd145human GRCh37 chr7: 91,033,585-91,042,496 , GRCh38.p12 chr7: 91,404,270-91,413,181 LINC02932
    nsv3116140copy number variation45nstd145human GRCh37 chr4: 21,369,066-21,376,838 , GRCh38.p12 chr4: 21,367,443-21,375,215 KCNIP4
    nsv3112700copy number variation32nstd145human GRCh37 chr12: 86,695,674-86,703,013 , GRCh38.p12 chr12: 86,301,896-86,309,235 MGAT4C
    nsv3117297copy number variation80nstd145human GRCh37 chr7: 154,392,836-154,399,317 , GRCh38.p12 chr7: 154,601,126-154,607,607 DPP6
    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
    nsv3112488copy number variation14nstd145human GRCh37 chr7: 16,794,950-16,800,421 , GRCh38.p12 chr7: 16,755,325-16,760,796 TSPAN13
    nsv3117385copy number variation76nstd145human GRCh37 chr7: 110,182,897-110,188,346 , GRCh38.p12 chr7: 110,542,840-110,548,289 LOC105375451
    nsv3113689copy number variation1nstd145human GRCh37 chr4: 7,866,493-7,871,827 , GRCh38.p12 chr4: 7,864,766-7,870,100 AFAP1
    nsv3117110copy number variation7nstd145human GRCh37 chr8: 87,188,232-87,193,436 , GRCh38.p12 chr8: 86,176,003-86,181,207 LOC105375623
    nsv3117560copy number variation15nstd145human GRCh37 chr4: 172,988,669-172,993,726 , GRCh38.p12 chr4: 172,067,518-172,072,575 GALNTL6
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