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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5926988copy number variation1nstd209human GRCh38 chr11: 117,310,194-117,312,213 , GRCh37.p13 chr11: 117,180,910-117,182,929 BACE1
    nsv5860144copy number variation1nstd209human GRCh38 chr11: 117,310,172-117,312,271 , GRCh37.p13 chr11: 117,180,888-117,182,987 BACE1
    nsv5513562copy number variation1nstd206human GRCh38 chr11: 117,310,673-117,329,839 , GRCh37.p13 chr11: 117,181,389-117,200,555 CEP164, BACE1
    nsv5502110copy number variation1nstd206human GRCh38 chr11: 117,310,197-117,312,214 , GRCh37.p13 chr11: 117,180,913-117,182,930 BACE1
    nsv5499739copy number variation1nstd206human GRCh38 chr11: 117,307,372-117,309,942 , GRCh37.p13 chr11: 117,178,088-117,180,658 BACE1
    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
    nsv5309857copy number variation1nstd204human GRCh38.p13 chr11: 117,309,962-117,312,525 , GRCh37.p13 chr11: 117,180,678-117,183,241 BACE1
    nsv5266255copy number variation1nstd204human GRCh38.p13 chr11: 117,310,001-117,312,500 , GRCh37.p13 chr11: 117,180,717-117,183,216 BACE1
    nsv5130984mobile element insertion1nstd203human GRCh38 chr11: 117,311,803-117,311,820 , GRCh37.p13 chr11: 117,182,519-117,182,536 BACE1
    nsv5128336mobile element insertion1nstd203human GRCh38 chr11: 117,311,787-117,311,803 , GRCh37.p13 chr11: 117,182,503-117,182,519 BACE1
    nsv5035338inversion1nstd200human GRCh38 chr11: 114,039,980-117,481,226 , GRCh37.p13 chr11: 113,910,702-117,351,941 , LINC02703, 56 more genes
    nsv4989338copy number variation1nstd200human GRCh38 chr11: 117,298,197-117,300,507 , GRCh37.p13 chr11: 117,168,913-117,171,223 BACE1
    nsv4837372copy number variation1nstd200human GRCh37 chr11: 117,180,913-117,182,930 , GRCh38.p12 chr11: 117,310,197-117,312,214 BACE1
    nsv4835607copy number variation1nstd200human GRCh37 chr11: 117,180,678-117,183,242 , GRCh38.p12 chr11: 117,309,962-117,312,526 BACE1
    nsv4732750copy number variation1nstd199human GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572 , LINC02702, 392 more genes
    nsv4674572copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 114,433,313-131,230,466 , GRCh38.p12 chr11: 114,562,591-131,360,571 ACRV1, APLP2, 382 more genes
    nsv4665918copy number variation1nstd186human GRCh37 chr11: 117,180,910-117,182,930 , GRCh38.p12 chr11: 117,310,194-117,312,214 BACE1
    nsv4614046copy number variation1nstd183human GRCh37 chr11: 117,180,910-117,182,930 , GRCh38.p12 chr11: 117,310,194-117,312,214 BACE1
    nsv4607621copy number variation1nstd183human GRCh37 chr11: 117,157,930-117,274,653 , GRCh38.p12 chr11: 117,287,214-117,403,937 BACE1, CEP164, 2 more genes
    nsv4431080copy number variation1nstd174human GRCh37 chr11: 117,180,910-117,182,968 , GRCh38.p12 chr11: 117,310,194-117,312,252 BACE1
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