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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5497791copy number variation1nstd206human GRCh38 chr11: 61,881,699-61,885,727 , GRCh37.p13 chr11: 61,649,171-61,653,199 FADS3
    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
    nsv4985001copy number variation1nstd200human GRCh38 chr11: 61,888,918-61,900,388 , GRCh37.p13 chr11: 61,656,390-61,667,860 FADS3, RAB3IL1
    nsv4979663copy number variation1nstd200human GRCh38 chr11: 61,884,596-61,885,570 , GRCh37.p13 chr11: 61,652,068-61,653,042 FADS3
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4675148copy number variation1nstd102humanUncertain significance GRCh37 chr11: 60,385,382-62,456,278 , GRCh38.p12 chr11: 60,617,909-62,688,806 LOC105369326, MS4A18, 91 more genes
    nsv4617422copy number variation1nstd183human GRCh37 chr11: 61,649,174-61,653,214 , GRCh38.p12 chr11: 61,881,702-61,885,742 FADS3
    nsv4192846copy number variation1nstd166human GRCh37.p13 chr11: 61,652,732-61,659,713 , GRCh38.p12 chr11: 61,885,260-61,892,241 FADS3
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 LOC105376598, OSBPL9P2, 2842 more genes
    nsv3890886copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 58,935,215-62,177,656 , GRCh38.p12 chr11: 59,167,742-62,410,184 MYRF, TMEM258, 137 more genes
    nsv3168425copy number variation1nstd158human GRCh37 chr11: 3,543,079-67,662,509 , GRCh38.p12 chr11: 3,521,849-67,895,038 , ACP2, 1535 more genes
    nsv3148943copy number variation1nstd151human GRCh37 chr11: 61,608,093-61,675,137 , GRCh38.p12 chr11: 61,840,621-61,907,665 FADS3, MIR6746, 2 more genes
    nsv3147762copy number variation1nstd151human GRCh37 chr11: 61,644,980-61,670,018 , GRCh38.p12 chr11: 61,877,508-61,902,546 RAB3IL1, FADS3, 1 more genes
    nsv2788088copy number variation1nstd132human NCBI36 chr11: 61,381,281-61,485,639 , GRCh37.p13 chr11: 61,624,705-61,729,063 , GRCh38.p12 chr11: 61,857,233-61,961,591 FADS3, RAB3IL1, 5 more genes
    nsv2786609copy number variation1nstd132human NCBI36 chr11: 61,381,281-61,435,152 , GRCh37.p13 chr11: 61,624,705-61,678,576 , GRCh38.p12 chr11: 61,857,233-61,911,104 FADS2, FADS3, 2 more genes
    esv3864264copy number variation1estd219human GRCh37 chr11: 61,649,171-61,653,219 , GRCh38.p12 chr11: 61,881,699-61,885,747 FADS3
    nsv2764126copy number variation1nstd130human GRCh37 chr11: 61,624,705-61,674,354 , GRCh38.p12 chr11: 61,857,233-61,906,882 FADS2, RAB3IL1, 2 more genes
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