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Items: 1 to 20 of 356

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979093inversion1nstd209human GRCh38 chr7: 150,023,235-154,074,108 , GRCh37.p13 chr7: 149,720,324-153,771,193 , AOC1, 98 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5491694copy number variation1nstd206human GRCh38 chr7: 151,112,827-151,113,207 , GRCh37.p13 chr7: 150,809,914-150,810,294 AGAP3
    nsv5381637copy number variation1nstd102humanUncertain significance GRCh37 chr7: 150,642,453-152,373,165 , GRCh38.p12 chr7: 150,945,365-152,676,080 WDR86-AS1, XRCC2, 44 more genes
    nsv5371381translocation1nstd200human GRCh38 chr7: 151,098,231-151,098,231 , GRCh38 chr7: 151,098,326-151,098,326 , GRCh37.p13 chr7: 150,795,318-150,795,318 , GRCh37.p13 chr7: 150,795,413-150,795,413 AGAP3
    nsv5332912translocation1nstd200human GRCh37 chr7: 150,795,413-150,795,413 , GRCh37 chr7: 150,795,318-150,795,318 , GRCh38.p12 chr7: 151,098,231-151,098,231 , GRCh38.p12 chr7: 151,098,326-151,098,326 AGAP3
    nsv5313617copy number variation1nstd204human GRCh38.p13 chr7: 151,109,099-151,109,196 , GRCh37.p13 chr7: 150,806,186-150,806,283 AGAP3
    nsv5309834copy number variation1nstd204human GRCh38.p13 chr7: 150,919,962-151,152,701 , GRCh37.p13 chr7: 150,617,050-150,849,788 , TMUB1, 10 more genes
    nsv5245468copy number variation1nstd204human GRCh38.p13 chr7: 151,115,992-151,151,788 , GRCh37.p13 chr7: 150,813,079-150,848,875 GBX1, AGAP3
    nsv5241955copy number variation1nstd204human GRCh38.p13 chr7: 151,115,701-151,152,300 , GRCh37.p13 chr7: 150,812,788-150,849,387 GBX1, AGAP3
    nsv5196145mobile element insertion1nstd203human GRCh38 chr7: 151,113,868-151,113,883 , GRCh37.p13 chr7: 150,810,955-150,810,970 AGAP3
    nsv4954075copy number variation1nstd200human GRCh38 chr7: 151,139,481-151,761,662 , GRCh37.p13 chr7: 150,836,568-151,458,748 ABCF2-H2BK1, MIR3907, 17 more genes
    nsv4954072copy number variation1nstd200human GRCh38 chr7: 150,920,190-151,152,443 , GRCh37.p13 chr7: 150,617,278-150,849,530 , TMUB1, 10 more genes
    nsv4951259copy number variation1nstd200human GRCh38 chr7: 151,109,102-151,109,194 , GRCh37.p13 chr7: 150,806,189-150,806,281 AGAP3
    nsv4951258copy number variation1nstd200human GRCh38 chr7: 151,104,943-151,106,489 , GRCh37.p13 chr7: 150,802,030-150,803,576 AGAP3
    nsv4825432copy number variation1nstd200human GRCh37 chr7: 150,617,278-150,849,530 , GRCh38.p12 chr7: 150,920,190-151,152,443 , FASTK, 10 more genes
    nsv4812438copy number variation1nstd200human GRCh37 chr7: 150,802,030-150,803,576 , GRCh38.p12 chr7: 151,104,943-151,106,489 AGAP3
    nsv4754093inversion1nstd199human GRCh37 chr7: 149,731,009-153,760,532 , GRCh38.p12 chr7: 150,033,920-154,063,447 , AOC1, 98 more genes
    nsv4685715copy number variation1nstd102humannot provided GRCh37 chr7: 143,107,740-156,886,246 , GRCh38.p12 chr7: 143,410,647-157,093,552 CTAGE4, CDK5, 277 more genes
    nsv4683838copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr7: 150,642,443-151,385,353 , GRCh38.p12 chr7: 150,945,355-151,688,267 CDK5, MIR3907, 26 more genes
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