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Items: 1 to 20 of 194

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5912158copy number variation1nstd209human GRCh38 chr9: 34,184,869-34,185,180 , GRCh37.p13 chr9: 34,184,867-34,185,178 UBAP1, LOC114224
    nsv5714340mobile element insertion1nstd211human GRCh38 chr9: 34,187,620-34,187,620 , GRCh37.p13 chr9: 34,187,618-34,187,618 LOC114224, UBAP1
    nsv5556974mobile element insertion1nstd206human GRCh38 chr9: 34,187,620-34,187,671 , GRCh37.p13 chr9: 34,187,618-34,187,669 UBAP1, LOC114224
    nsv5490552copy number variation1nstd206human GRCh38 chr9: 34,183,831-34,188,257 , GRCh37.p13 chr9: 34,183,829-34,188,255 UBAP1, LOC114224
    nsv5485932copy number variation1nstd206human GRCh38 chr9: 34,184,645-34,192,502 , GRCh37.p13 chr9: 34,184,643-34,192,500 UBAP1, LOC114224, 1 more genes
    nsv5485919copy number variation1nstd206human GRCh38 chr9: 33,787,875-34,192,689 , GRCh37.p13 chr9: 33,787,873-34,192,687 LOC114224, TUBB4BP2, 14 more genes
    nsv5316458copy number variation1nstd204human GRCh37.p13 chr9: 34,183,819-34,188,264 , GRCh38.p13 chr9: 34,183,821-34,188,266 LOC114224, UBAP1
    nsv5250040copy number variation1nstd204human GRCh38.p13 chr9: 33,851,001-34,396,200 , GRCh37.p13 chr9: 33,850,999-34,396,198 KIF24, SERPINH1P1, 22 more genes
    nsv5241017copy number variation1nstd204human GRCh38.p13 chr9: 34,185,066-34,186,965 , GRCh37.p13 chr9: 34,185,064-34,186,963 LOC114224, UBAP1
    nsv5190810mobile element insertion1nstd203human GRCh38 chr9: 34,187,620-34,187,620 , GRCh37.p13 chr9: 34,187,618-34,187,618 UBAP1, LOC114224
    nsv4964269copy number variation1nstd200human GRCh38 chr9: 34,183,646-34,187,933 , GRCh37.p13 chr9: 34,183,644-34,187,931 UBAP1, LOC114224
    nsv4954658copy number variation1nstd200human GRCh38 chr9: 34,141,862-34,214,698 , GRCh37.p13 chr9: 34,141,860-34,214,696 RPL35AP2, LOC114224, 2 more genes
    nsv4954657copy number variation1nstd200human GRCh38 chr9: 34,103,197-34,805,619 , GRCh37.p13 chr9: 34,103,195-34,805,616 , CCL27, 32 more genes
    nsv4828232copy number variation1nstd200human GRCh37 chr9: 34,183,828-34,188,256 , GRCh38.p12 chr9: 34,183,830-34,188,258 LOC114224, UBAP1
    nsv4828231copy number variation1nstd200human GRCh37 chr9: 34,183,644-34,187,931 , GRCh38.p12 chr9: 34,183,646-34,187,933 UBAP1, LOC114224
    nsv4814744copy number variation1nstd200human GRCh37 chr9: 34,141,859-34,214,696 , GRCh38.p12 chr9: 34,141,861-34,214,698 RPL35AP2, LOC114224, 2 more genes
    nsv4814740copy number variation1nstd200human GRCh37 chr9: 33,787,873-34,192,687 , GRCh38.p12 chr9: 33,787,875-34,192,689 UBE2R2, PRSS3, 14 more genes
    nsv4766654inversion1nstd199human GRCh37 chr9: 201,453-68,434,063 , GRCh38.p12 chr9: 201,453-67,920,552 , ACO1, 876 more genes
    nsv4755256inversion1nstd199human GRCh37 chr9: 200,777-70,835,468 , GRCh38.p12 chr9: 200,777-67,920,552 , ACO1, 876 more genes
    nsv4729230copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 32,192,406-38,311,776 , GRCh38.p12 chr9: 32,192,408-38,311,779 ACO1, ANXA2P2, 210 more genes
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