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Items: 1 to 20 of 1022

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5967354insertion1nstd209human GRCh38 chr4: 123,096,242-123,096,242 , GRCh37.p13 chr4: 124,017,397-124,017,397 AFG2A
    nsv5958046insertion1nstd209human GRCh38 chr4: 122,994,723-122,994,723 , GRCh37.p13 chr4: 123,915,878-123,915,878 AFG2A
    nsv5957630insertion1nstd209human GRCh38 chr4: 123,108,260-123,108,260 , GRCh37.p13 chr4: 124,029,415-124,029,415 AFG2A
    nsv5955899insertion1nstd209human GRCh38 chr4: 123,118,316-123,118,316 , GRCh37.p13 chr4: 124,039,471-124,039,471 AFG2A
    nsv5904567copy number variation1nstd209human GRCh38 chr4: 123,134,911-123,134,966 , GRCh37.p13 chr4: 124,056,066-124,056,121 AFG2A
    nsv5899510copy number variation1nstd209human GRCh38 chr4: 123,052,145-123,054,931 , GRCh37.p13 chr4: 123,973,300-123,976,086 AFG2A
    nsv5891043copy number variation1nstd209human GRCh38 chr4: 123,173,146-123,230,593 , GRCh37.p13 chr4: 124,094,301-124,151,748 AFG2A
    nsv5889832copy number variation1nstd209human GRCh38 chr4: 123,184,529-123,184,640 , GRCh37.p13 chr4: 124,105,684-124,105,795 AFG2A
    nsv5837876copy number variation1nstd209human GRCh38 chr4: 123,187,210-123,188,509 , GRCh37.p13 chr4: 124,108,365-124,109,664 AFG2A
    nsv5837646copy number variation1nstd209human GRCh38 chr4: 123,211,642-123,213,041 , GRCh37.p13 chr4: 124,132,797-124,134,196 AFG2A
    nsv5837609copy number variation2nstd209human GRCh38 chr4: 123,223,139-123,224,138 , GRCh37.p13 chr4: 124,144,294-124,145,293 AFG2A
    nsv5837608copy number variation1nstd209human GRCh38 chr4: 123,172,626-123,231,656 , GRCh37.p13 chr4: 124,093,781-124,152,811 AFG2A
    nsv5837338copy number variation1nstd209human GRCh38 chr4: 123,205,442-123,206,441 , GRCh37.p13 chr4: 124,126,597-124,127,596 AFG2A
    nsv5837337copy number variation1nstd209human GRCh38 chr4: 123,052,086-123,054,985 , GRCh37.p13 chr4: 123,973,241-123,976,140 AFG2A
    nsv5837336copy number variation1nstd209human GRCh38 chr4: 123,001,927-123,004,008 , GRCh37.p13 chr4: 123,923,082-123,925,163 AFG2A
    nsv5725444mobile element insertion1nstd211human GRCh38 chr4: 123,273,076-123,273,076 , GRCh37.p13 chr4: 124,194,231-124,194,231 AFG2A
    nsv5693209mobile element insertion1nstd211human GRCh38 chr4: 123,306,284-123,306,284 , GRCh37.p13 chr4: 124,227,439-124,227,439 AFG2A
    nsv5690625mobile element insertion1nstd211human GRCh38 chr4: 123,082,001-123,082,001 , GRCh37.p13 chr4: 124,003,156-124,003,156 AFG2A
    nsv5689138mobile element insertion1nstd211human GRCh38 chr4: 122,921,130-122,921,130 , GRCh37.p13 chr4: 123,842,285-123,842,285 AFG2A, NUDT6
    nsv5680279mobile element insertion1nstd211human GRCh38 chr4: 123,144,868-123,144,868 , GRCh37.p13 chr4: 124,066,023-124,066,023 AFG2A
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