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Items: 1 to 20 of 247

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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
    nsv5929615copy number variation1nstd209human GRCh38 chr15: 75,884,893-75,885,358 , GRCh37.p13 chr15: 76,177,234-76,177,699 UBE2Q2
    nsv5848544copy number variation1nstd209human GRCh38 chr15: 75,881,786-75,886,222 , GRCh37.p13 chr15: 76,174,127-76,178,563 UBE2Q2
    nsv5527248copy number variation1nstd206human GRCh38 chr15: 75,884,926-75,885,359 , GRCh37.p13 chr15: 76,177,267-76,177,700 UBE2Q2
    nsv5515822copy number variation1nstd206human GRCh38 chr15: 75,873,752-75,883,686 , GRCh37.p13 chr15: 76,166,093-76,176,027 UBE2Q2
    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
    nsv5147983mobile element insertion1nstd203human GRCh38 chr15: 75,864,935-75,864,946 , GRCh37.p13 chr15: 76,157,276-76,157,287 UBE2Q2
    nsv5037756inversion1nstd200human GRCh38 chr15: 75,735,812-77,868,882 , GRCh37.p13 chr15: 76,028,153-78,161,224 TRK-CTT16-1, SCAPER, 34 more genes
    nsv4992298copy number variation1nstd200human GRCh38 chr15: 73,152,590-82,101,178 , GRCh37.p13 chr15: 73,444,931-82,393,519 , SNUPN, 215 more genes
    nsv4850134copy number variation1nstd200human GRCh37 chr15: 76,177,260-76,177,700 , GRCh38.p12 chr15: 75,884,919-75,885,359 UBE2Q2
    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
    nsv4629779copy number variation1nstd183human GRCh37 chr15: 76,149,653-76,152,381 , GRCh38.p12 chr15: 75,857,312-75,860,040 UBE2Q2
    nsv4628111copy number variation1nstd183human GRCh37 chr15: 76,146,915-76,152,381 , GRCh38.p12 chr15: 75,854,574-75,860,040 UBE2Q2
    nsv4627861copy number variation1nstd183human GRCh37 chr15: 76,146,968-76,152,381 , GRCh38.p12 chr15: 75,854,627-75,860,040 UBE2Q2
    nsv4624026copy number variation1nstd183human GRCh37 chr15: 76,120,924-76,228,892 , GRCh38.p12 chr15: 75,828,583-75,936,551 FBXO22, UBE2Q2, 2 more genes
    nsv4621725copy number variation1nstd183human GRCh37 chr15: 76,166,043-76,176,013 , GRCh38.p12 chr15: 75,873,702-75,883,672 UBE2Q2
    nsv4619530copy number variation1nstd183human GRCh37 chr15: 76,171,353-76,175,807 , GRCh38.p12 chr15: 75,879,012-75,883,466 UBE2Q2
    nsv4532244copy number variation1nstd166human GRCh37.p13 chr15: 76,164,965-76,165,054 , GRCh38.p12 chr15: 75,872,624-75,872,713 UBE2Q2
    nsv4515141mobile element insertion1nstd166human GRCh37.p13 chr15: 76,156,492-76,156,492 , GRCh38.p12 chr15: 75,864,151-75,864,151 UBE2Q2
    nsv4506308mobile element insertion1nstd166human GRCh37.p13 chr15: 76,192,224-76,192,224 , GRCh38.p12 chr15: 75,899,883-75,899,883 UBE2Q2
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