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Items: 1 to 20 of 585

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5969069insertion1nstd209human GRCh38 chr15: 36,703,219-36,703,219 , GRCh37.p13 chr15: 36,995,420-36,995,420 CDIN1
    nsv5936009copy number variation1nstd209human GRCh38 chr15: 36,662,440-36,662,491 , GRCh37.p13 chr15: 36,954,641-36,954,692 CDIN1
    nsv5935085copy number variation1nstd209human GRCh38 chr15: 36,751,090-36,751,167 , GRCh37.p13 chr15: 37,043,291-37,043,368 CDIN1
    nsv5707054mobile element insertion1nstd211human GRCh38 chr15: 36,686,872-36,686,872 , GRCh37.p13 chr15: 36,979,073-36,979,073 CDIN1
    nsv5701774mobile element insertion1nstd211human GRCh38 chr15: 36,702,215-36,702,215 , GRCh37.p13 chr15: 36,994,416-36,994,416 CDIN1
    nsv5700794mobile element insertion2nstd211human GRCh38 chr15: 36,743,321-36,743,321 , GRCh37.p13 chr15: 37,035,522-37,035,522 CDIN1
    nsv5646436insertion1nstd207human GRCh38 chr15: 36,703,219-36,703,219 , GRCh37.p13 chr15: 36,995,420-36,995,420 CDIN1
    nsv5602767copy number variation1nstd207human GRCh38 chr15: 36,800,871-36,800,932 , GRCh37.p13 chr15: 37,093,072-37,093,133 CDIN1, CSNK1A1P1
    nsv5599374copy number variation1nstd207human GRCh38 chr15: 36,703,341-36,703,404 , GRCh37.p13 chr15: 36,995,542-36,995,605 CDIN1
    nsv5593080copy number variation1nstd207human GRCh38 chr15: 36,662,440-36,662,491 , GRCh37.p13 chr15: 36,954,641-36,954,692 CDIN1
    nsv5512650copy number variation1nstd206human GRCh38 chr15: 36,751,093-36,751,169 , GRCh37.p13 chr15: 37,043,294-37,043,370 CDIN1
    nsv5503612copy number variation1nstd206human GRCh38 chr15: 36,703,350-36,703,409 , GRCh37.p13 chr15: 36,995,551-36,995,610 CDIN1
    nsv5495660copy number variation1nstd206human GRCh38 chr15: 36,727,875-36,727,947 , GRCh37.p13 chr15: 37,020,076-37,020,148 CDIN1
    nsv5422823mobile element insertion1nstd206human GRCh38 chr15: 36,743,321-36,743,372 , GRCh37.p13 chr15: 37,035,522-37,035,573 CDIN1
    nsv5420537mobile element insertion1nstd206human GRCh38 chr15: 36,702,215-36,702,266 , GRCh37.p13 chr15: 36,994,416-36,994,467 CDIN1
    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
    nsv5380028translocation1nstd200human GRCh38 chr15: 36,758,934-36,758,934 , GRCh38 chr15: 36,764,682-36,764,682 , GRCh37.p13 chr15: 37,051,135-37,051,135 , GRCh37.p13 chr15: 37,056,883-37,056,883 CDIN1
    nsv5380027translocation1nstd200human GRCh38 chr15: 36,636,368-36,636,368 , GRCh38 chr15: 36,625,194-36,625,194 , GRCh37.p13 chr15: 36,917,395-36,917,395 , GRCh37.p13 chr15: 36,928,569-36,928,569 CDIN1, TPST2P1
    nsv5361712translocation1nstd200human GRCh38 chr15: 36,698,801-36,698,801 , GRCh38 chr3: 82,095,596-82,095,596 , GRCh37.p13 chr15: 36,991,002-36,991,002 , GRCh37.p13 chr3: 82,144,747-82,144,747 CDIN1, LINC02008
    nsv5357804translocation1nstd200human GRCh38 chr15: 36,764,426-36,764,426 , GRCh38 chr15: 36,758,936-36,758,936 , GRCh37.p13 chr15: 37,056,627-37,056,627 , GRCh37.p13 chr15: 37,051,137-37,051,137 CDIN1
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