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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3114198copy number variation1nstd145human GRCh37 chr5: 106,336,524-106,421,432 , GRCh38.p12 chr5: 107,000,823-107,085,731 LINC01950
    nsv3116050copy number variation42nstd145human GRCh37 chr14: 41,610,263-41,668,279 , GRCh38.p12 chr14: 41,141,060-41,199,076 LINC02315
    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
    nsv3117809copy number variation152nstd145human GRCh37 chr20: 1,561,593-1,584,273 , GRCh38.p12 chr20: 1,580,947-1,603,627 SIRPB1
    nsv3116181copy number variation1nstd145human GRCh37 chr3: 164,539,221-164,555,283 , GRCh38.p12 chr3: 164,821,433-164,837,495 LINC01324
    nsv3115825copy number variation6nstd145human GRCh37 chr16: 12,414,529-12,428,826 , GRCh38.p12 chr16: 12,320,672-12,334,969 SNX29
    nsv3113350copy number variation3nstd145human GRCh37 chr1: 169,229,179-169,240,805 , GRCh38.p12 chr1: 169,259,941-169,271,567 NME7
    nsv3116107copy number variation1nstd145human GRCh37 chr13: 63,281,436-63,292,072 , GRCh38.p12 chr13: 62,707,303-62,717,939 LINC00448
    nsv3116640copy number variation17nstd145human GRCh37 chr3: 192,875,554-192,884,946 , GRCh38.p12 chr3: 193,157,765-193,167,157 VEZF1P1
    nsv3112490copy number variation2nstd145human GRCh37 chr11: 55,422,322-55,431,504 , GRCh38.p12 chr11: 55,654,846-55,664,028 OR4C6
    nsv3116948copy number variation9nstd145human GRCh37 chr11: 55,434,691-55,443,378 , GRCh38.p12 chr11: 55,667,215-55,675,902 OR4V1P
    nsv3113895copy number variation1nstd145human GRCh37 chr3: 37,978,379-37,985,910 , GRCh38.p12 chr3: 37,936,888-37,944,419 CTDSPL
    nsv3112146copy number variation37nstd145human GRCh37 chr11: 93,695,236-93,701,577 , GRCh38.p12 chr11: 93,962,070-93,968,411 LOC101060084
    nsv3114208copy number variation43nstd145human GRCh37 chr3: 189,364,561-189,370,847 , GRCh38.p12 chr3: 189,646,772-189,653,058 TP63
    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
    nsv3113599copy number variation29nstd145human GRCh37 chr4: 122,282,472-122,288,171 , GRCh38.p12 chr4: 121,361,317-121,367,016 QRFPR
    nsv3112010copy number variation1nstd145human GRCh37 chr11: 5,802,634-5,808,269 , GRCh38.p12 chr11: 5,781,404-5,787,039 OR52N1
    nsv3113954copy number variation1nstd145human GRCh37 chr1: 35,106,706-35,112,001 , GRCh38.p12 chr1: 34,641,105-34,646,400 LOC105378641
    nsv3111268copy number variation1nstd145human GRCh37 chr8: 51,032,366-51,037,344 , GRCh38.p12 chr8: 50,119,806-50,124,784 SNTG1
    nsv3114178copy number variation107nstd145human GRCh37 chr6: 53,928,991-53,933,879 , GRCh38.p12 chr6: 54,064,193-54,069,081 MLIP
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