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Items: 1 to 20 of 367

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5958902insertion1nstd209human GRCh38 chr9: 97,815,306-97,815,306 , GRCh37.p13 chr9: 100,577,588-100,577,588 PTCSC2
    nsv5958766insertion1nstd209human GRCh38 chr9: 97,779,561-97,779,561 , GRCh37.p13 chr9: 100,541,843-100,541,843 PTCSC2
    nsv5709742mobile element insertion2nstd211human GRCh38 chr9: 97,826,278-97,826,278 , GRCh37.p13 chr9: 100,588,560-100,588,560 PTCSC2
    nsv5695579mobile element insertion2nstd211human GRCh38 chr9: 97,850,379-97,850,379 , GRCh37.p13 chr9: 100,612,661-100,612,661 PTCSC2
    nsv5629904insertion1nstd207human GRCh38 chr9: 97,742,220-97,742,220 , GRCh37.p13 chr9: 100,504,502-100,504,502 PTCSC2
    nsv5586235copy number variation1nstd207human GRCh38 chr9: 97,796,926-97,797,023 , GRCh37.p13 chr9: 100,559,208-100,559,305 PTCSC2
    nsv5550238insertion1nstd206human GRCh38 chr9: 97,815,629-97,815,664 , GRCh37.p13 chr9: 100,577,911-100,577,946 PTCSC2
    nsv5493743copy number variation1nstd206human GRCh38 chr9: 97,799,651-97,800,422 , GRCh37.p13 chr9: 100,561,933-100,562,704 PTCSC2
    nsv5481338copy number variation1nstd206human GRCh38 chr9: 97,730,043-97,730,150 , GRCh37.p13 chr9: 100,492,325-100,492,432 PTCSC2
    nsv5481039copy number variation1nstd206human GRCh38 chr9: 97,739,566-97,739,652 , GRCh37.p13 chr9: 100,501,848-100,501,934 PTCSC2
    nsv5480186copy number variation1nstd206human GRCh38 chr9: 97,843,743-97,844,053 , GRCh37.p13 chr9: 100,606,025-100,606,335 PTCSC2
    nsv5412236mobile element insertion1nstd206human GRCh38 chr9: 97,850,379-97,850,430 , GRCh37.p13 chr9: 100,612,661-100,612,712 PTCSC2
    nsv5404187mobile element insertion1nstd206human GRCh38 chr9: 97,826,278-97,826,329 , GRCh37.p13 chr9: 100,588,560-100,588,611 PTCSC2
    nsv5381561copy number variation1nstd102humanPathogenic GRCh37 chr9: 97,834,573-107,199,088 , GRCh38.p12 chr9: 95,072,291-104,436,807 TBC1D2, ZNF782, 170 more genes
    nsv5372863translocation1nstd200human GRCh38 chr9: 97,844,053-97,844,053 , GRCh38 chr9: 97,843,743-97,843,743 , GRCh37.p13 chr9: 100,606,025-100,606,025 , GRCh37.p13 chr9: 100,606,335-100,606,335 PTCSC2
    nsv5330212translocation1nstd200human GRCh37 chr9: 100,492,432-100,492,432 , GRCh37 chr9: 100,492,325-100,492,325 , GRCh38.p12 chr9: 97,730,043-97,730,043 , GRCh38.p12 chr9: 97,730,150-97,730,150 PTCSC2
    nsv5309619copy number variation1nstd204human GRCh38.p13 chr9: 97,843,733-97,844,062 , GRCh37.p13 chr9: 100,606,015-100,606,344 PTCSC2
    nsv5184662mobile element insertion1nstd203human GRCh38 chr9: 97,828,566-97,828,579 , GRCh37.p13 chr9: 100,590,848-100,590,861 PTCSC2
    nsv5184602mobile element insertion1nstd203human GRCh38 chr9: 97,828,570-97,828,579 , GRCh37.p13 chr9: 100,590,852-100,590,861 PTCSC2
    nsv5130959mobile element insertion1nstd203human GRCh38 chr9: 97,815,613-97,815,629 , GRCh37.p13 chr9: 100,577,895-100,577,911 PTCSC2
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