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Items: 1 to 20 of 439

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5924585copy number variation1nstd209human GRCh38 chr7: 135,096,480-135,096,662 , GRCh37.p13 chr7: 134,781,232-134,781,414 AGBL3, CYREN
    nsv5908964copy number variation1nstd209human GRCh38 chr7: 135,024,814-135,028,411 , GRCh37.p13 chr7: 134,709,565-134,713,162 AGBL3
    nsv5853809copy number variation1nstd209human GRCh38 chr7: 135,024,860-135,028,407 , GRCh37.p13 chr7: 134,709,611-134,713,158 AGBL3
    nsv5850371copy number variation1nstd209human GRCh38 chr7: 135,099,649-135,100,948 , GRCh37.p13 chr7: 134,784,401-134,785,700 CYREN, AGBL3
    nsv5716091mobile element insertion2nstd211human GRCh38 chr7: 134,998,796-134,998,796 , GRCh37.p13 chr7: 134,683,547-134,683,547 AGBL3
    nsv5710543mobile element insertion2nstd211human GRCh38 chr7: 135,079,082-135,079,082 , GRCh37.p13 chr7: 134,763,834-134,763,834 AGBL3
    nsv5707623mobile element insertion1nstd211human GRCh38 chr7: 135,062,071-135,062,071 , GRCh37.p13 chr7: 134,746,822-134,746,822 AGBL3
    nsv5570448copy number variation1nstd207human GRCh38 chr7: 135,024,814-135,028,409 , GRCh37.p13 chr7: 134,709,565-134,713,160 AGBL3
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5482532copy number variation1nstd206human GRCh38 chr7: 135,025,668-135,025,755 , GRCh37.p13 chr7: 134,710,419-134,710,506 AGBL3
    nsv5479120copy number variation1nstd206human GRCh38 chr7: 135,024,814-135,028,412 , GRCh37.p13 chr7: 134,709,565-134,713,163 AGBL3
    nsv5479062copy number variation1nstd206human GRCh38 chr7: 135,127,228-135,127,288 , GRCh37.p13 chr7: 134,811,980-134,812,040 AGBL3, RNF14P4, 1 more genes
    nsv5478627copy number variation1nstd206human GRCh38 chr7: 135,013,610-135,014,311 , GRCh37.p13 chr7: 134,698,361-134,699,062 AGBL3
    nsv5476963copy number variation1nstd206human GRCh38 chr7: 135,019,551-135,020,108 , GRCh37.p13 chr7: 134,704,302-134,704,859 AGBL3
    nsv5475643copy number variation1nstd206human GRCh38 chr7: 135,001,394-135,011,662 , GRCh37.p13 chr7: 134,686,145-134,696,413 AGBL3
    nsv5407044mobile element insertion1nstd206human GRCh38 chr7: 135,062,071-135,062,122 , GRCh37.p13 chr7: 134,746,822-134,746,873 AGBL3
    nsv5403504mobile element insertion1nstd206human GRCh38 chr7: 135,079,082-135,079,126 , GRCh37.p13 chr7: 134,763,834-134,763,878 AGBL3
    nsv5371246translocation1nstd200human GRCh38 chr7: 135,013,610-135,013,610 , GRCh38 chr7: 135,014,382-135,014,382 , GRCh37.p13 chr7: 134,698,361-134,698,361 , GRCh37.p13 chr7: 134,699,133-134,699,133 AGBL3
    nsv5336678translocation1nstd200human GRCh37 chr7: 134,698,361-134,698,361 , GRCh37 chr7: 134,699,133-134,699,133 , GRCh38.p12 chr7: 135,013,610-135,013,610 , GRCh38.p12 chr7: 135,014,382-135,014,382 AGBL3
    nsv5331108translocation1nstd200human GRCh37 chr7: 134,772,535-134,772,535 , GRCh37 chr7: 134,772,444-134,772,444 , GRCh38.p12 chr7: 135,087,692-135,087,692 , GRCh38.p12 chr7: 135,087,783-135,087,783 AGBL3
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