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Items: 1 to 20 of 220

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5918182copy number variation1nstd209human GRCh38 chr7: 16,643,503-16,643,960 , GRCh37.p13 chr7: 16,683,128-16,683,585 ANKMY2
    nsv5715376mobile element insertion2nstd211human GRCh38 chr7: 16,621,693-16,621,693 , GRCh37.p13 chr7: 16,661,318-16,661,318 ANKMY2
    nsv5642035insertion1nstd207human GRCh38 chr7: 16,627,957-16,627,957 , GRCh37.p13 chr7: 16,667,582-16,667,582 ANKMY2
    nsv5640228insertion1nstd207human GRCh38 chr7: 16,627,732-16,627,732 , GRCh37.p13 chr7: 16,667,357-16,667,357 ANKMY2
    nsv5578569copy number variation1nstd207human GRCh38 chr7: 16,627,732-16,627,830 , GRCh37.p13 chr7: 16,667,357-16,667,455 ANKMY2
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5554657mobile element insertion1nstd206human GRCh38 chr7: 16,621,693-16,621,744 , GRCh37.p13 chr7: 16,661,318-16,661,369 ANKMY2
    nsv5457464copy number variation1nstd206human GRCh38 chr7: 16,643,507-16,643,961 , GRCh37.p13 chr7: 16,683,132-16,683,586 ANKMY2
    nsv5388754copy number variation2nstd186human GRCh37 chr7: 16,683,132-16,683,586 , GRCh38.p12 chr7: 16,643,507-16,643,961 ANKMY2
    nsv5370329translocation1nstd200human GRCh38 chr7: 16,624,226-16,624,226 , GRCh38 chr7: 16,624,130-16,624,130 , GRCh37.p13 chr7: 16,663,755-16,663,755 , GRCh37.p13 chr7: 16,663,851-16,663,851 ANKMY2
    nsv5337116translocation1nstd200human GRCh37 chr7: 16,663,755-16,663,755 , GRCh37 chr7: 16,663,851-16,663,851 , GRCh38.p12 chr7: 16,624,130-16,624,130 , GRCh38.p12 chr7: 16,624,226-16,624,226 ANKMY2
    nsv5317634copy number variation1nstd204human GRCh38.p13 chr7: 16,080,765-17,645,128 , GRCh37.p13 chr7: 16,120,390-17,684,752 AHR, RAD17P1, 23 more genes
    nsv5309399copy number variation1nstd204human GRCh38.p13 chr7: 16,517,170-17,062,629 , GRCh37.p13 chr7: 16,556,795-17,102,253 ANKMY2, LOC100287613, 11 more genes
    nsv5234826copy number variation1nstd204human GRCh38.p13 chr7: 16,517,201-17,062,700 , GRCh37.p13 chr7: 16,556,826-17,102,324 RAD17P1, BZW2, 11 more genes
    nsv5234141copy number variation1nstd204human GRCh38.p13 chr7: 16,639,801-16,640,800 , GRCh37.p13 chr7: 16,679,426-16,680,425 ANKMY2
    nsv5232226copy number variation1nstd204human GRCh38.p13 chr7: 16,626,156-16,630,933 , GRCh37.p13 chr7: 16,665,781-16,670,558 ANKMY2
    nsv5226353copy number variation1nstd204human GRCh38.p13 chr7: 16,612,921-16,649,596 , GRCh37.p13 chr7: 16,652,546-16,689,221 ANKMY2, LOC105375169, 1 more genes
    nsv5224947copy number variation1nstd204human GRCh38.p13 chr7: 16,594,745-16,601,862 , GRCh37.p13 chr7: 16,634,370-16,641,487 ANKMY2
    nsv5223578copy number variation1nstd204human GRCh38.p13 chr7: 16,522,001-17,645,100 , GRCh37.p13 chr7: 16,561,626-17,684,724 LOC105375172, LOC105375169, 18 more genes
    nsv5220943copy number variation1nstd204human GRCh38.p13 chr7: 16,584,610-16,616,444 , GRCh37.p13 chr7: 16,624,235-16,656,069 LOC105375169, ANKMY2, 1 more genes
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