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Items: 1 to 20 of 155

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978819inversion1nstd209human GRCh38 chr15: 81,455,809-83,007,946 , GRCh37.p13 chr15: 81,748,150-83,676,698 RPS17, AP3B2, 39 more genes
    nsv5529424copy number variation1nstd206human GRCh38 chr15: 82,593,088-82,725,956 , GRCh37.p13 chr15: 83,295,965-83,394,708 AP3B2, CPEB1, 4 more genes
    nsv5514636copy number variation1nstd206human GRCh38 chr15: 82,628,241-82,789,039 , GRCh37.p13 chr15: 83,296,992-83,457,791 AP3B2, CPEB1, 7 more genes
    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
    nsv5304944copy number variation1nstd204human GRCh38.p13 chr15: 82,628,238-82,789,048 , GRCh37.p13 chr15: 83,296,989-83,457,800 AP3B2, CPEB1, 7 more genes
    nsv5304530copy number variation1nstd204human GRCh38.p13 chr15: 82,713,096-82,718,032 , GRCh37.p13 chr15: 83,381,848-83,386,784 LOC338963
    nsv5280153copy number variation1nstd204human GRCh38.p13 chr15: 82,712,985-82,718,259 , GRCh37.p13 chr15: 83,381,737-83,387,011 LOC338963
    nsv5273623copy number variation1nstd204human GRCh38.p13 chr15: 82,712,401-82,717,800 , GRCh37.p13 chr15: 83,381,153-83,386,552 LOC338963
    nsv5272449copy number variation1nstd204human GRCh37.p13 chr15: 83,297,052-83,457,752 , GRCh38.p13 chr15: 82,628,301-82,789,000 AP3B2, CPEB1, 7 more genes
    nsv5262982copy number variation1nstd204human GRCh38.p13 chr15: 82,705,543-82,742,917 , GRCh37.p13 chr15: 83,374,295-83,411,669 LOC338963, ACTG1P17, 1 more genes
    nsv5002038copy number variation1nstd200human GRCh38 chr15: 82,628,241-82,789,039 , GRCh37.p13 chr15: 83,296,992-83,457,791 AP3B2, CPEB1, 7 more genes
    nsv4863917copy number variation1nstd200human GRCh37 chr15: 83,381,955-83,386,659 , GRCh38.p12 chr15: 82,713,203-82,717,907 LOC338963
    nsv4856079copy number variation1nstd200human GRCh37 chr15: 83,296,992-83,457,791 , GRCh38.p12 chr15: 82,641,775-82,789,039 AP3B2, CPEB1, 7 more genes
    nsv4729284copy number variation1nstd102humanPathogenic GRCh37 chr15: 83,201,955-85,786,847 , GRCh38.p12 chr15: 82,641,775-85,243,616 GOLGA6L5P, DNM1P44, 77 more genes
    nsv4619968copy number variation1nstd183human GRCh37 chr15: 83,245,326-83,468,089 , GRCh38.p12 chr15: 82,641,775-82,799,337 AP3B2, CPEB1, 7 more genes
    nsv4578262copy number variation1nstd102humanPathogenic GRCh37 chr15: 83,214,012-84,772,030 , GRCh38.p12 chr15: 82,641,775-84,103,278 LOC100421235, LOC105370933, 29 more genes
    nsv4456897copy number variation1nstd102humanUncertain significance GRCh37 chr15: 82,468,371-84,797,068 , GRCh38.p12 chr15: 82,176,030-84,128,316 HDGFL3, LOC105370926, 46 more genes
    nsv4456639copy number variation1nstd102humanPathogenic GRCh37 chr15: 80,728,654-84,107,646 , GRCh38.p12 chr15: 80,436,313-83,438,894 LOC100288241, LOC105370926, 64 more genes
    nsv4455892copy number variation1nstd102humanPathogenic GRCh37 chr15: 82,688,216-84,796,779 , GRCh38.p12 chr15: 82,396,005-84,128,027 UBE2Q2P2, GOLGA2P10, 40 more genes
    nsv4425568copy number variation1nstd174human GRCh37 chr15: 83,237,514-83,472,507 , GRCh38.p12 chr15: 82,641,775-82,803,755 AP3B2, CPEB1, 7 more genes
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