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Items: 1 to 20 of 165

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5902991copy number variation1nstd209human GRCh38 chr3: 109,176,658-109,176,708 , GRCh37.p13 chr3: 108,895,505-108,895,555 LINC00488
    nsv5834261copy number variation1nstd209human GRCh38 chr3: 109,165,072-109,199,615 , GRCh37.p13 chr3: 108,883,919-108,918,462 LINC00488
    nsv5833921copy number variation2nstd209human GRCh38 chr3: 109,171,906-109,177,373 , GRCh37.p13 chr3: 108,890,753-108,896,220 LINC00488
    nsv5444773copy number variation1nstd206human GRCh38 chr3: 108,753,574-109,201,574 , GRCh37.p13 chr3: 108,472,421-108,920,421 GUCA1C, MORC1, 5 more genes
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4914621copy number variation1nstd200human GRCh38 chr3: 109,126,812-109,248,675 , GRCh37.p13 chr3: 108,845,659-108,967,522 C3orf85, RNU6-1236P, 2 more genes
    nsv4794279copy number variation1nstd200human GRCh37 chr3: 108,845,659-108,967,522 , GRCh38.p12 chr3: 109,126,812-109,248,675 C3orf85, RNU6-1236P, 2 more genes
    nsv4794278copy number variation1nstd200human GRCh37 chr3: 108,417,663-108,975,570 , GRCh38.p12 chr3: 108,698,816-109,256,723 LOC105374034, BRD7P7, 9 more genes
    nsv4680907copy number variation1nstd189human GRCh37.p13 chr3: 108,601,809-109,000,461 , GRCh38.p12 chr3: 108,882,962-109,281,614 GUCA1C, MORC1, 5 more genes
    nsv4680857copy number variation1nstd189human GRCh37.p13 chr3: 108,601,809-109,015,183 , GRCh38.p12 chr3: 108,882,962-109,296,336 GUCA1C, MORC1, 6 more genes
    nsv4674516copy number variation1nstd102humanUncertain significance GRCh37 chr3: 108,848,313-108,936,533 , GRCh38.p12 chr3: 109,129,466-109,217,686 C3orf85, LINC00488
    nsv4674342copy number variation1nstd102humanUncertain significance GRCh37 chr3: 108,483,112-108,911,182 , GRCh38.p12 chr3: 108,764,265-109,192,335 LINC00488, MORC1-AS1, 4 more genes
    nsv4674254copy number variation1nstd102humanPathogenic GRCh37 chr3: 101,812,245-112,174,485 , GRCh38.p12 chr3: 102,093,401-112,455,638 IFT57, LINC00636, 111 more genes
    nsv4587004copy number variation1nstd183human GRCh37 chr3: 108,597,736-109,015,183 , GRCh38.p12 chr3: 108,878,889-109,296,336 GUCA1C, MORC1, 6 more genes
    nsv4584881copy number variation1nstd183human GRCh37 chr3: 108,848,505-108,895,592 , GRCh38.p12 chr3: 109,129,658-109,176,745 C3orf85, LINC00488
    nsv4317801inversion1nstd166human GRCh37.p13 chr3: 106,160,269-123,476,086 , GRCh38.p12 chr3: 106,441,422-123,757,239 , ADPRH, 270 more genes
    nsv4085421copy number variation1nstd166human GRCh37.p13 chr3: 108,845,629-108,967,522 , GRCh38.p12 chr3: 109,126,782-109,248,675 BRD7P7, LINC00488, 2 more genes
    nsv4079060copy number variation1nstd166human GRCh37.p13 chr3: 108,352,740-111,211,030 , GRCh38.p12 chr3: 108,633,893-111,492,183 , ATP6V0CP2, 30 more genes
    nsv4073356copy number variation1nstd166human GRCh37.p13 chr3: 108,597,026-109,016,388 , GRCh38.p12 chr3: 108,878,179-109,297,541 GUCA1C, MORC1, 6 more genes
    nsv3971198copy number variation1nstd168human GRCh38 chr3: 109,181,594-109,208,403 , GRCh37.p13 chr3: 108,900,441-108,927,250 LINC00488
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