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Items: 1 to 20 of 192

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5933606copy number variation1nstd209human GRCh38 chr15: 71,577,714-80,433,232 , GRCh37.p13 chr15: 71,870,053-80,725,573 , STRA6, 229 more genes
    nsv5931219copy number variation1nstd209human GRCh38 chr15: 75,682,165-75,682,282 , GRCh37.p13 chr15: 75,974,506-75,974,623 CSPG4
    nsv5928357copy number variation1nstd209human GRCh38 chr15: 75,270,339-75,786,969 , GRCh37.p13 chr15: 75,562,680-76,079,310 LOC101929408, RN7SL319P, 23 more genes
    nsv5714292mobile element insertion2nstd211human GRCh38 chr15: 75,675,573-75,675,573 , GRCh37.p13 chr15: 75,967,914-75,967,914 CSPG4
    nsv5662209insertion1nstd207human GRCh38 chr15: 75,699,121-75,699,121 , GRCh37.p13 chr15: 75,991,462-75,991,462 CSPG4
    nsv5657863insertion1nstd207human GRCh38 chr15: 75,686,044-75,686,044 , GRCh37.p13 chr15: 75,978,385-75,978,385 CSPG4
    nsv5650922insertion1nstd207human GRCh38 chr15: 75,685,082-75,685,082 , GRCh37.p13 chr15: 75,977,423-75,977,423 CSPG4
    nsv5646627insertion1nstd207human GRCh38 chr15: 75,688,159-75,688,159 , GRCh37.p13 chr15: 75,980,500-75,980,500 CSPG4
    nsv5595410copy number variation1nstd207human GRCh38 chr15: 75,681,214-75,681,283 , GRCh37.p13 chr15: 75,973,555-75,973,624 CSPG4
    nsv5588961copy number variation1nstd207human GRCh38 chr15: 75,701,222-75,701,287 , GRCh37.p13 chr15: 75,993,563-75,993,628 CSPG4
    nsv5588308copy number variation1nstd207human GRCh38 chr15: 75,712,783-75,714,084 , GRCh37.p13 chr15: 76,005,124-76,006,425 CSPG4
    nsv5532876copy number variation1nstd206human GRCh38 chr15: 75,680,731-75,682,110 , GRCh37.p13 chr15: 75,973,072-75,974,451 CSPG4
    nsv5428252mobile element insertion1nstd206human GRCh38 chr15: 75,675,573-75,675,624 , GRCh37.p13 chr15: 75,967,914-75,967,965 CSPG4
    nsv5380975copy number variation1nstd102humanPathogenic GRCh37 chr15: 75,596,353-76,103,430 , GRCh38.p12 chr15: 75,304,012-75,811,089 RPL13P4, PTPN9, 20 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
    nsv5001783copy number variation1nstd200human GRCh38 chr15: 75,707,843-75,710,565 , GRCh37.p13 chr15: 76,000,184-76,002,906 CSPG4
    nsv5001782copy number variation1nstd200human GRCh38 chr15: 75,680,773-75,682,061 , GRCh37.p13 chr15: 75,973,114-75,974,402 CSPG4
    nsv4992298copy number variation1nstd200human GRCh38 chr15: 73,152,590-82,101,178 , GRCh37.p13 chr15: 73,444,931-82,393,519 , SNUPN, 215 more genes
    nsv4850132copy number variation1nstd200human GRCh37 chr15: 75,973,114-75,974,402 , GRCh38.p12 chr15: 75,680,773-75,682,061 CSPG4
    nsv4729733copy number variation1nstd102humanUncertain significance GRCh37 chr15: 75,920,400-76,632,051 , GRCh38.p12 chr15: 75,628,059-76,339,710 ISL2, TYRO3P, 18 more genes
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