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Items: 1 to 20 of 263

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5958328insertion1nstd209human GRCh38 chr9: 94,454,529-94,454,529 , GRCh37.p13 chr9: 97,216,811-97,216,811 MFSD14B
    nsv5911418copy number variation1nstd209human GRCh38 chr9: 94,452,697-94,452,746 , GRCh37.p13 chr9: 97,214,979-97,215,028 MFSD14B
    nsv5866569copy number variation1nstd209human GRCh38 chr9: 94,394,951-94,397,082 , GRCh37.p13 chr9: 97,157,233-97,159,364 MFSD14B
    nsv5861971copy number variation1nstd209human GRCh38 chr9: 94,378,034-94,380,867 , GRCh37.p13 chr9: 97,140,316-97,143,149 MFSD14B
    nsv5861684copy number variation1nstd209human GRCh38 chr9: 94,394,017-94,397,082 , GRCh37.p13 chr9: 97,156,299-97,159,364 MFSD14B
    nsv5856558copy number variation1nstd209human GRCh38 chr9: 94,388,795-94,392,492 , GRCh37.p13 chr9: 97,151,077-97,154,774 MFSD14B
    nsv5723677mobile element insertion1nstd211human GRCh38 chr9: 94,392,811-94,392,811 , GRCh37.p13 chr9: 97,155,093-97,155,093 MFSD14B
    nsv5698454mobile element insertion1nstd211human GRCh38 chr9: 94,428,568-94,428,568 , GRCh37.p13 chr9: 97,190,850-97,190,850 MFSD14B
    nsv5635627insertion1nstd207human GRCh38 chr9: 94,454,529-94,454,529 , GRCh37.p13 chr9: 97,216,811-97,216,811 MFSD14B
    nsv5624538insertion1nstd207human GRCh38 chr9: 94,382,940-94,382,940 , GRCh37.p13 chr9: 97,145,222-97,145,222 MFSD14B
    nsv5595177copy number variation1nstd207human GRCh38 chr9: 94,452,687-94,452,746 , GRCh37.p13 chr9: 97,214,969-97,215,028 MFSD14B
    nsv5591893copy number variation1nstd207human GRCh38 chr9: 94,438,761-94,438,885 , GRCh37.p13 chr9: 97,201,043-97,201,167 MFSD14B
    nsv5586464copy number variation1nstd207human GRCh38 chr9: 94,438,767-94,439,115 , GRCh37.p13 chr9: 97,201,049-97,201,397 MFSD14B
    nsv5561778mobile element insertion1nstd206human GRCh38 chr9: 94,392,811-94,392,857 , GRCh37.p13 chr9: 97,155,093-97,155,139 MFSD14B
    nsv5540466insertion1nstd206human GRCh38 chr9: 94,454,546-94,454,580 , GRCh37.p13 chr9: 97,216,828-97,216,862 MFSD14B
    nsv5535496insertion1nstd206human GRCh38 chr9: 94,446,730-94,446,767 , GRCh37.p13 chr9: 97,209,012-97,209,049 MFSD14B
    nsv5489937copy number variation1nstd206human GRCh38 chr9: 94,412,552-94,428,552 , GRCh37.p13 chr9: 97,174,834-97,190,834 MFSD14B
    nsv5489379copy number variation1nstd206human GRCh38 chr9: 94,392,552-94,398,552 , GRCh37.p13 chr9: 97,154,834-97,160,834 MFSD14B
    nsv5488368copy number variation1nstd206human GRCh38 chr9: 94,460,625-94,463,841 , GRCh37.p13 chr9: 97,222,907-97,226,123 MFSD14B
    nsv5481729copy number variation1nstd206human GRCh38 chr9: 94,404,572-94,407,623 , GRCh37.p13 chr9: 97,166,854-97,169,905 MFSD14B
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