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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv3904761copy number variation1nstd102humanPathogenic GRCh37 chr11: 80,053,454-113,316,236 , GRCh38.p12 chr11: 80,342,410-113,445,514 RPS6P16, CTSC, 449 more genes
    nsv3917126copy number variation1nstd102humanPathogenic GRCh38 chr4: 116,630,862-145,429,900 , NCBI36 chr4: 117,771,466-146,570,502 , GRCh37 chr4: 117,552,018-146,351,052 CLGN, SETD7, 294 more genes
    nsv3913977copy number variation1nstd102humanPathogenic GRCh37 chr11: 77,943,882-106,650,146 , GRCh38 chr11: 78,232,836-106,779,420 , NCBI36 chr11: 77,621,530-106,155,356 PLS1P1, SNORA25, 349 more genes
    nsv3910101copy number variation1nstd102humanPathogenic NCBI36 chr11: 87,796,211-113,996,548 , GRCh37.p13 chr11: 88,156,563-114,491,338 , GRCh38.p12 chr11: 88,423,395-114,620,616 PHB1P16, LOC100418884, 385 more genes
    nsv6637396copy number variation1nstd102humanPathogenic GRCh37 chr11: 81,478,509-104,667,040 , GRCh38.p12 chr11: 81,767,467-104,796,313 LOC107984375, RN7SL222P, 295 more genes
    nsv3894488copy number variation1nstd102humanPathogenic GRCh37 chr11: 88,152,458-109,414,650 , GRCh38.p12 chr11: 88,419,290-109,543,924 RNU6-16P, DDX10, 270 more genes
    nsv3910663copy number variation1nstd102humanPathogenic GRCh38 chr11: 91,086,659-109,595,582 , NCBI36 chr11: 90,459,475-108,971,518 , GRCh37 chr11: 90,819,827-109,466,308 LOC101060084, PGAM1P9, 230 more genes
    nsv3922508copy number variation1nstd102humanPathogenic GRCh38 chr11: 85,242,847-102,920,097 , GRCh37 chr11: 84,953,891-102,738,968 , NCBI36 chr11: 84,631,539-102,296,037 AMOTL1, LNCRNA-IUR, 240 more genes
    nsv5672640copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976 HSPD1P13, CARD17P, 239 more genes
    nsv3874323copy number variation1nstd102humanPathogenic GRCh37 chr4: 126,549,693-141,313,049 , GRCh38.p12 chr4: 125,628,538-140,391,895 CLGN, FTH1P24, 127 more genes
    nsv3912421copy number variation1nstd102humanPathogenic NCBI36 chr4: 129,260,477-143,571,978 , GRCh37 chr4: 129,041,027-143,352,528 , GRCh38 chr4: 128,119,872-142,431,375 CLGN, PCDH10-DT, 120 more genes
    nsv6637687copy number variation1nstd102humanPathogenic GRCh37 chr11: 101,371,503-109,306,519 , GRCh38.p12 chr11: 101,500,772-109,435,793 GRIA4, MTND1P36, 111 more genes
    nsv3924464copy number variation1nstd102humanPathogenic NCBI36 chr11: 97,733,839-105,435,083 , GRCh38 chr11: 98,357,901-106,059,146 , GRCh37 chr11: 98,228,629-105,929,873 ARHGAP42, PDGFDDN, 91 more genes
    nsv6291168copy number variation1nstd102humanPathogenic GRCh37 chr4: 138,289,049-145,923,298 , GRCh38.p12 chr4: 137,367,895-145,002,146 CLGN, LOC105377447, 92 more genes
    nsv4674499copy number variation1nstd102humanPathogenic GRCh37 chr4: 139,531,815-146,095,109 , GRCh38.p12 chr4: 138,610,661-145,173,957 CLGN, GUSBP5, 77 more genes
    nsv6290718copy number variation1nstd102humanPathogenic GRCh37 chr4: 136,529,470-141,564,812 , GRCh38.p12 chr4: 135,608,315-140,643,658 CLGN, MGARP, 61 more genes
    nsv4674743copy number variation1nstd102humanPathogenic GRCh37 chr4: 137,901,978-141,527,647 , GRCh38.p12 chr4: 136,980,824-140,606,493 CLGN, RAB33B-AS1, 56 more genes
    nsv6309019copy number variation2nstd102humanPathogenic GRCh37 chr11: 101,323,686-103,349,981 , GRCh38.p12 chr11: 101,452,955-103,479,253 RPL21P96, RNU6-952P, 40 more genes
    nsv3873978copy number variation1nstd102humanPathogenic GRCh37 chr4: 11,525-191,028,879 , GRCh38.p12 chr4: 11,525-190,107,724 CLGN, LOC100422029, 2358 more genes
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