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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5863175copy number variation1nstd209human GRCh38 chr11: 94,641,721-94,647,075 , GRCh37.p13 chr11: 94,374,887-94,380,241 PIWIL4-AS1, LINC02700
    nsv5858515copy number variation1nstd209human GRCh38 chr11: 94,643,846-94,648,084 , GRCh37.p13 chr11: 94,377,012-94,381,250 PIWIL4-AS1, LINC02700
    nsv5850886copy number variation1nstd209human GRCh38 chr11: 94,640,641-94,643,545 , GRCh37.p13 chr11: 94,373,807-94,376,711 LINC02700, PIWIL4-AS1
    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
    nsv5510599copy number variation1nstd206human GRCh38 chr11: 94,641,843-94,647,162 , GRCh37.p13 chr11: 94,375,009-94,380,328 LINC02700, PIWIL4-AS1
    nsv5495130copy number variation1nstd206human GRCh38 chr11: 94,651,112-94,651,462 , GRCh37.p13 chr11: 94,384,278-94,384,628 LINC02700, PIWIL4-AS1
    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
    nsv5037979inversion1nstd200human GRCh38 chr11: 93,899,952-96,855,215 , GRCh37.p13 chr11: 93,633,118-96,726,215 , GPR83, 52 more genes
    nsv4989179copy number variation1nstd200human GRCh38 chr11: 94,641,843-94,646,765 , GRCh37.p13 chr11: 94,375,009-94,379,931 PIWIL4-AS1, LINC02700
    nsv4971715copy number variation1nstd200human GRCh38 chr11: 94,588,056-94,730,817 , GRCh37.p13 chr11: 94,321,222-94,463,983 PIWIL4-AS1, PIWIL4, 2 more genes
    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
    nsv4837450copy number variation1nstd200human GRCh37 chr11: 94,374,958-94,380,346 , GRCh38.p12 chr11: 94,641,792-94,647,180 PIWIL4-AS1, LINC02700
    nsv4499271mobile element insertion1nstd166human GRCh37.p13 chr11: 94,372,053-94,372,053 , GRCh38.p12 chr11: 94,638,887-94,638,887 PIWIL4-AS1, LINC02700
    nsv4207661copy number variation1nstd166human GRCh37.p13 chr11: 94,374,950-94,380,000 , GRCh38.p12 chr11: 94,641,784-94,646,834 LINC02700, PIWIL4-AS1
    nsv4197084copy number variation1nstd166human GRCh37.p13 chr11: 94,375,061-94,379,875 , GRCh38.p12 chr11: 94,641,895-94,646,709 PIWIL4-AS1, LINC02700
    nsv4195824copy number variation1nstd166human GRCh37.p13 chr11: 94,375,043-94,380,213 , GRCh38.p12 chr11: 94,641,877-94,647,047 LINC02700, PIWIL4-AS1
    nsv4195500copy number variation1nstd166human GRCh37.p13 chr11: 94,384,278-94,384,628 , GRCh38.p12 chr11: 94,651,112-94,651,462 PIWIL4-AS1, LINC02700
    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
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