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Items: 1 to 20 of 140

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6512377copy number variation1nstd223human GRCh38 chr15: 48,187,801-48,188,700 , GRCh37.p13 chr15: 48,479,998-48,480,897 CTXN2-AS1, CTXN2
    nsv6509009copy number variation1nstd223human GRCh38 chr15: 48,197,757-48,198,128 , GRCh37.p13 chr15: 48,489,954-48,490,325 CTXN2
    nsv6505870copy number variation1nstd223human GRCh38 chr15: 48,197,401-48,198,800 , GRCh37.p13 chr15: 48,489,598-48,490,997 CTXN2
    nsv6500422copy number variation1nstd223human GRCh38 chr15: 48,196,101-48,198,600 , GRCh37.p13 chr15: 48,488,298-48,490,797 CTXN2
    nsv6313917copy number variation1nstd102humanPathogenic GRCh37 chr15: 47,635,238-56,509,908 , GRCh38.p12 chr15: 47,343,041-56,217,710 PYGO1, RNU6-449P, 125 more genes
    nsv6309791copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,426,485-48,730,124 , GRCh38.p12 chr15: 48,134,288-48,437,927 DUT, FBN1, 6 more genes
    nsv6291817copy number variation1nstd102humanUncertain significance GRCh37 chr15: 48,149,321-48,522,259 , GRCh38.p12 chr15: 47,857,124-48,230,062 SLC24A5, LOC102724553, 6 more genes
    nsv6291615copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,179,968-48,727,846 , GRCh38.p12 chr15: 47,887,771-48,435,649 LOC102724553, CTXN2-AS1, 9 more genes
    nsv5522030copy number variation1nstd206human GRCh38 chr15: 48,188,983-48,192,234 , GRCh37.p13 chr15: 48,481,180-48,484,431 CTXN2, CTXN2-AS1
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv5001681copy number variation1nstd200human GRCh38 chr15: 47,881,221-48,441,463 , GRCh37.p13 chr15: 48,173,418-48,733,660 , 14 more genes
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4866068copy number variation1nstd200human GRCh37 chr15: 48,173,418-48,733,660 , GRCh38.p12 chr15: 47,881,221-48,441,463 , FBN1, 14 more genes
    nsv4682714copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,426,485-48,936,976 , GRCh38.p12 chr15: 48,134,288-48,644,779 DUT, FBN1, 7 more genes
    nsv4675095copy number variation1nstd102humanPathogenic GRCh37 chr15: 47,192,561-50,819,726 , GRCh38.p12 chr15: 46,900,363-50,527,529 LOC102724587, LOC645405, 51 more genes
    nsv4506491mobile element insertion1nstd166human GRCh37.p13 chr15: 48,477,432-48,477,432 , GRCh38.p12 chr15: 48,185,235-48,185,235 CTXN2-AS1, CTXN2
    nsv4456196copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,000,433-60,747,551 , GRCh38.p12 chr15: 47,708,236-60,455,352 MIR1266, AQP9, 199 more genes
    nsv4451860copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,051,994-48,830,007 , GRCh38.p12 chr15: 47,759,797-48,537,810 SLC12A1, FBN1, 11 more genes
    nsv4335090sequence alteration1nstd166human GRCh37.p13 chr15: 48,474,857-48,484,898 , GRCh38.p12 chr15: 48,182,660-48,192,701 CTXN2, CTXN2-AS1
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