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Items: 1 to 20 of 281

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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
    nsv5913135copy number variation1nstd209human GRCh38 chr7: 151,360,895-151,361,038 , GRCh37.p13 chr7: 151,057,981-151,058,124 NUB1
    nsv5908708copy number variation1nstd209human GRCh38 chr7: 151,344,739-151,344,871 , GRCh37.p13 chr7: 151,041,825-151,041,957 NUB1
    nsv5908313copy number variation1nstd209human GRCh38 chr7: 151,344,137-151,344,955 , GRCh37.p13 chr7: 151,041,223-151,042,041 NUB1
    nsv5716978mobile element insertion1nstd211human GRCh38 chr7: 151,371,356-151,371,356 , GRCh37.p13 chr7: 151,068,442-151,068,442 NUB1
    nsv5696803mobile element insertion2nstd211human GRCh38 chr7: 151,365,004-151,365,004 , GRCh37.p13 chr7: 151,062,090-151,062,090 NUB1
    nsv5630708insertion1nstd207human GRCh38 chr7: 151,364,974-151,364,974 , GRCh37.p13 chr7: 151,062,060-151,062,060 NUB1
    nsv5569880copy number variation1nstd207human GRCh38 chr7: 151,360,895-151,361,038 , GRCh37.p13 chr7: 151,057,981-151,058,124 NUB1
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5491306copy number variation1nstd206human GRCh38 chr7: 151,344,739-151,344,886 , GRCh37.p13 chr7: 151,041,825-151,041,972 NUB1
    nsv5484006copy number variation1nstd206human GRCh38 chr7: 151,280,443-151,375,576 , GRCh37.p13 chr7: 150,977,529-151,072,662 NUB1
    nsv5483920copy number variation1nstd206human GRCh38 chr7: 151,360,921-151,361,033 , GRCh37.p13 chr7: 151,058,007-151,058,119 NUB1
    nsv5399047mobile element insertion1nstd206human GRCh38 chr7: 151,365,004-151,365,055 , GRCh37.p13 chr7: 151,062,090-151,062,141 NUB1
    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
    nsv5338035translocation1nstd200human GRCh37 chr7: 151,058,119-151,058,119 , GRCh37 chr7: 151,058,007-151,058,007 , GRCh38.p12 chr7: 151,360,921-151,360,921 , GRCh38.p12 chr7: 151,361,033-151,361,033 NUB1
    nsv5321953translocation1nstd204human GRCh38.p13 chr7: 151,360,921-151,360,921 , GRCh38.p13 chr7: 151,361,033-151,361,033 , GRCh37.p13 chr7: 151,058,007-151,058,007 , GRCh37.p13 chr7: 151,058,119-151,058,119 NUB1
    nsv5319110copy number variation1nstd204human GRCh38.p13 chr7: 151,315,012-151,349,917 , GRCh37.p13 chr7: 151,012,098-151,047,003 NUB1
    nsv5255275copy number variation1nstd204human GRCh38.p13 chr7: 151,341,381-151,346,931 , GRCh37.p13 chr7: 151,038,467-151,044,017 NUB1
    nsv5245573copy number variation1nstd204human GRCh38.p13 chr7: 151,312,408-151,342,875 , GRCh37.p13 chr7: 151,009,494-151,039,961 NUB1
    nsv5245419copy number variation1nstd204human GRCh38.p13 chr7: 151,316,601-151,363,900 , GRCh37.p13 chr7: 151,013,687-151,060,986 NUB1
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