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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5511708copy number variation1nstd206human GRCh38 chr11: 94,376,171-94,376,288 , GRCh37.p13 chr11: 94,109,337-94,109,454 GPR83
    nsv5501054copy number variation1nstd206human GRCh38 chr11: 94,374,439-94,390,344 , GRCh37.p13 chr11: 94,107,605-94,123,510 GPR83
    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
    nsv5307911copy number variation1nstd204human GRCh38.p13 chr11: 94,374,478-94,390,369 , GRCh37.p13 chr11: 94,107,644-94,123,535 GPR83
    nsv5261810copy number variation1nstd204human GRCh38.p13 chr11: 94,376,385-94,388,386 , GRCh37.p13 chr11: 94,109,551-94,121,552 GPR83
    nsv5037979inversion1nstd200human GRCh38 chr11: 93,899,952-96,855,215 , GRCh37.p13 chr11: 93,633,118-96,726,215 , GPR83, 52 more genes
    nsv4971707copy number variation1nstd200human GRCh38 chr11: 94,389,180-94,391,390 , GRCh37.p13 chr11: 94,122,346-94,124,556 GPR83
    nsv4971706copy number variation1nstd200human GRCh38 chr11: 94,383,856-94,387,700 , GRCh37.p13 chr11: 94,117,022-94,120,866 GPR83
    nsv4971705copy number variation1nstd200human GRCh38 chr11: 94,374,485-94,390,362 , GRCh37.p13 chr11: 94,107,651-94,123,528 GPR83
    nsv4971591copy number variation1nstd200human GRCh38 chr11: 91,285,470-94,799,390 , GRCh37.p13 chr11: 91,018,638-94,532,556 , LOC105369429, 53 more genes
    nsv4839969copy number variation1nstd200human GRCh37 chr11: 91,018,638-94,532,556 , GRCh38.p12 chr11: 91,285,470-94,799,390 , MIR548L, 53 more genes
    nsv4830796copy number variation1nstd200human GRCh37 chr11: 94,107,651-94,123,528 , GRCh38.p12 chr11: 94,374,485-94,390,362 GPR83
    nsv4748487copy number variation1nstd199human GRCh37 chr11: 94,109,333-94,109,452 , GRCh38.p12 chr11: 94,376,167-94,376,286 GPR83
    nsv4729076copy number variation1nstd102humanUncertain significance GRCh37 chr11: 93,676,223-94,342,737 , GRCh38.p12 chr11: 93,943,057-94,609,571 HEPHL1, ARPC3P3, 14 more genes
    nsv4381135copy number variation1nstd173human GRCh37 chr11: 94,102,184-94,126,708 , GRCh38.p12 chr11: 94,369,018-94,393,542 GPR83
    nsv4200350copy number variation1nstd166human GRCh37.p13 chr11: 94,114,309-94,114,377 , GRCh38.p12 chr11: 94,381,143-94,381,211 GPR83
    nsv4192822copy number variation1nstd166human GRCh37.p13 chr11: 94,108,684-94,128,294 , GRCh38.p12 chr11: 94,375,518-94,395,128 GPR83
    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
    nsv3921121copy number variation1nstd102humanPathogenic GRCh38 chr11: 75,941,754-98,357,960 , NCBI36 chr11: 75,330,446-97,733,898 , GRCh37 chr11: 75,652,798-98,228,688 LOC105369441, RNU6-1135P, 296 more genes
    nsv3916760copy number variation1nstd102humanUncertain significance NCBI36 chr11: 93,697,096-95,454,478 , GRCh38 chr11: 94,324,282-96,081,666 , GRCh37 chr11: 94,057,448-95,814,830 SESN3, SRSF8BP, 36 more genes
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