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Items: 1 to 20 of 339

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973938inversion1nstd209human GRCh38 chr8: 41,482,982-43,307,552 , GRCh37.p13 chr8: 41,340,501-43,162,695 , ANK1, 46 more genes
    nsv5948128insertion1nstd209human GRCh38 chr8: 42,054,252-42,054,252 , GRCh37.p13 chr8: 41,911,770-41,911,770 KAT6A-AS1
    nsv5919703copy number variation1nstd209human GRCh38 chr8: 42,081,963-42,091,008 , GRCh37.p13 chr8: 41,939,481-41,948,526 KAT6A-AS1
    nsv5917461copy number variation1nstd209human GRCh38 chr8: 41,299,580-47,196,853 , GRCh37.p13 chr8: 41,157,099-48,108,476 , AFG3L2P1, 81 more genes
    nsv5912359copy number variation1nstd209human GRCh38 chr8: 42,072,730-42,073,044 , GRCh37.p13 chr8: 41,930,248-41,930,562 KAT6A-AS1
    nsv5909297copy number variation1nstd209human GRCh38 chr8: 42,098,506-42,098,592 , GRCh37.p13 chr8: 41,956,024-41,956,110 KAT6A-AS1
    nsv5908388copy number variation1nstd209human GRCh38 chr8: 42,078,069-42,078,220 , GRCh37.p13 chr8: 41,935,587-41,935,738 KAT6A-AS1
    nsv5855816copy number variation1nstd209human GRCh38 chr8: 42,081,927-42,087,263 , GRCh37.p13 chr8: 41,939,445-41,944,781 KAT6A-AS1
    nsv5731010mobile element insertion1nstd211human GRCh38 chr8: 42,088,193-42,088,193 , GRCh37.p13 chr8: 41,945,711-41,945,711 KAT6A-AS1
    nsv5570767copy number variation1nstd207human GRCh38 chr8: 42,072,730-42,073,044 , GRCh37.p13 chr8: 41,930,248-41,930,562 KAT6A-AS1
    nsv5564499copy number variation1nstd102humanUncertain significance GRCh37 chr8: 41,905,876-42,188,497 , GRCh38.p12 chr8: 42,048,358-42,330,979 LOC101059972, IKBKB-DT, 8 more genes
    nsv5488670copy number variation1nstd206human GRCh38 chr8: 42,072,747-42,073,045 , GRCh37.p13 chr8: 41,930,265-41,930,563 KAT6A-AS1
    nsv5482154copy number variation1nstd206human GRCh38 chr8: 42,079,472-42,080,990 , GRCh37.p13 chr8: 41,936,990-41,938,508 KAT6A-AS1
    nsv5478451copy number variation1nstd206human GRCh38 chr8: 42,059,452-42,085,599 , GRCh37.p13 chr8: 41,916,970-41,943,117 KAT6A-AS1
    nsv5477220copy number variation1nstd206human GRCh38 chr8: 42,079,087-42,079,521 , GRCh37.p13 chr8: 41,936,605-41,937,039 KAT6A-AS1
    nsv5384143mobile element deletion2nstd186human GRCh37 chr8: 41,930,265-41,930,563 , GRCh38.p12 chr8: 42,072,747-42,073,045 KAT6A-AS1
    nsv5364146translocation1nstd200human GRCh38 chr8: 42,082,004-42,082,004 , GRCh38 chr8: 42,091,009-42,091,009 , GRCh37.p13 chr8: 41,939,522-41,939,522 , GRCh37.p13 chr8: 41,948,527-41,948,527 KAT6A-AS1
    nsv5212630mobile element deletion1nstd204human GRCh38.p13 chr8: 42,072,747-42,073,045 , GRCh37.p13 chr8: 41,930,265-41,930,563 KAT6A-AS1
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv5117187mobile element insertion1nstd203human GRCh38 chr8: 42,087,172-42,087,187 , GRCh37.p13 chr8: 41,944,690-41,944,705 KAT6A-AS1
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