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Items: 1 to 20 of 246

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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
    nsv5917636copy number variation1nstd209human GRCh38 chr7: 151,276,145-151,276,385 , GRCh37.p13 chr7: 150,973,231-150,973,471 SMARCD3
    nsv5561877sequence alteration1nstd206human GRCh38 chr7: 151,257,468-151,258,508 , GRCh37.p13 chr7: 150,954,554-150,955,594 SMARCD3
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    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
    nsv5301818copy number variation1nstd204human GRCh38.p13 chr7: 151,256,150-151,256,451 , GRCh37.p13 chr7: 150,953,236-150,953,537 SMARCD3
    nsv5116739mobile element insertion1nstd203human GRCh38 chr7: 151,259,822-151,259,843 , GRCh37.p13 chr7: 150,956,908-150,956,929 SMARCD3
    nsv5102703mobile element insertion1nstd203human GRCh38 chr7: 151,259,776-151,259,822 , GRCh37.p13 chr7: 150,956,862-150,956,908 SMARCD3
    nsv4954077copy number variation1nstd200human GRCh38 chr7: 151,258,347-151,259,267 , GRCh37.p13 chr7: 150,955,433-150,956,353 SMARCD3
    nsv4954076copy number variation1nstd200human GRCh38 chr7: 151,240,472-151,280,655 , GRCh37.p13 chr7: 150,937,558-150,977,741 SMARCD3
    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
    nsv4951262copy number variation1nstd200human GRCh38 chr7: 151,249,217-151,249,300 , GRCh37.p13 chr7: 150,946,303-150,946,386 SMARCD3
    nsv4825434copy number variation1nstd200human GRCh37 chr7: 150,955,424-150,956,361 , GRCh38.p12 chr7: 151,258,338-151,259,275 SMARCD3
    nsv4812440copy number variation1nstd200human GRCh37 chr7: 150,953,258-150,953,508 , GRCh38.p12 chr7: 151,256,172-151,256,422 SMARCD3
    nsv4812439copy number variation1nstd200human GRCh37 chr7: 150,946,303-150,946,386 , GRCh38.p12 chr7: 151,249,217-151,249,300 SMARCD3
    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
    nsv4675620copy number variation1nstd102humanPathogenic GRCh37 chr7: 109,251,060-159,119,707 , GRCh38.p12 chr7: 109,611,003-159,327,017 RPL26P23, ST13P17, 887 more genes
    nsv4675615copy number variation1nstd102humanPathogenic GRCh37 chr7: 131,414,604-159,126,310 , GRCh38.p12 chr7: 131,729,845-159,333,620 ATG9B, OR10AC1, 603 more genes
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