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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5917204copy number variation1nstd209human GRCh38 chr7: 54,772,149-54,772,220 , GRCh37.p13 chr7: 54,839,842-54,839,913 SEC61G-DT
    nsv5915764copy number variation1nstd209human GRCh38 chr7: 54,798,057-54,798,376 , GRCh37.p13 chr7: 54,865,750-54,866,069 SEC61G-DT
    nsv5721986mobile element insertion1nstd211human GRCh38 chr7: 54,788,243-54,788,243 , GRCh37.p13 chr7: 54,855,936-54,855,936 SEC61G-DT
    nsv5568082copy number variation1nstd207human GRCh38 chr7: 54,772,150-54,772,222 , GRCh37.p13 chr7: 54,839,843-54,839,915 SEC61G-DT
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5554702sequence alteration1nstd206human GRCh38 chr7: 54,775,168-54,777,171 , GRCh37.p13 chr7: 54,842,861-54,844,864 SEC61G-DT
    nsv5492608copy number variation1nstd206human GRCh38 chr7: 54,772,149-54,772,229 , GRCh37.p13 chr7: 54,839,842-54,839,922 SEC61G-DT
    nsv5484725copy number variation1nstd206human GRCh38 chr7: 54,805,346-54,805,433 , GRCh37.p13 chr7: 54,873,039-54,873,126 SEC61G-DT
    nsv5478327copy number variation1nstd206human GRCh38 chr7: 54,791,566-54,791,617 , GRCh37.p13 chr7: 54,859,259-54,859,310 SEC61G-DT
    nsv5477764copy number variation1nstd206human GRCh38 chr7: 54,798,504-54,798,562 , GRCh37.p13 chr7: 54,866,197-54,866,255 SEC61G-DT
    nsv5363682translocation1nstd200human GRCh38 chr7: 54,798,562-54,798,562 , GRCh38 chr7: 54,798,504-54,798,504 , GRCh37.p13 chr7: 54,866,197-54,866,197 , GRCh37.p13 chr7: 54,866,255-54,866,255 SEC61G-DT
    nsv5363681translocation1nstd200human GRCh38 chr7: 54,789,130-54,789,130 , GRCh38 chr7: 54,789,665-54,789,665 , GRCh37.p13 chr7: 54,856,823-54,856,823 , GRCh37.p13 chr7: 54,857,358-54,857,358 SEC61G-DT
    nsv5363680translocation1nstd200human GRCh38 chr7: 54,772,149-54,772,149 , GRCh38 chr7: 54,772,229-54,772,229 , GRCh37.p13 chr7: 54,839,842-54,839,842 , GRCh37.p13 chr7: 54,839,922-54,839,922 SEC61G-DT
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4956810copy number variation1nstd200human GRCh38 chr7: 54,777,452-54,783,888 , GRCh37.p13 chr7: 54,845,145-54,851,581 SEC61G-DT
    nsv4956809copy number variation1nstd200human GRCh38 chr7: 54,763,408-54,768,026 , GRCh37.p13 chr7: 54,831,101-54,835,719 SEC61G-DT
    nsv4953710copy number variation1nstd200human GRCh38 chr7: 54,583,600-55,152,153 , GRCh37.p13 chr7: 54,651,293-55,219,846 SEC61G, SEC61G-DT, 5 more genes
    nsv4828951copy number variation1nstd200human GRCh37 chr7: 54,651,293-55,219,846 , GRCh38.p12 chr7: 54,583,600-55,152,153 EGFR, LOC643168, 5 more genes
    nsv4819005copy number variation1nstd200human GRCh37 chr7: 54,856,823-54,857,358 , GRCh38.p12 chr7: 54,789,130-54,789,665 SEC61G-DT
    nsv4649575copy number variation1nstd186human GRCh37 chr7: 54,839,841-54,839,922 , GRCh38.p12 chr7: 54,772,148-54,772,229 SEC61G-DT
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