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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6115094mobile element insertion1nstd186human GRCh37 chr16: 2,412,367-2,412,367 , GRCh38.p12 chr16: 2,362,366-2,362,366 ABCA17P
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
    nsv5979983insertion1nstd209human GRCh38 chr16: 2,390,702-2,390,702 , GRCh37.p13 chr16: 2,440,703-2,440,703 ABCA17P
    nsv5977650insertion1nstd209human GRCh38 chr16: 2,404,822-2,404,822 , GRCh37.p13 chr16: 2,454,823-2,454,823 ABCA17P
    nsv5975479insertion1nstd209human GRCh38 chr16: 2,362,366-2,362,366 , GRCh37.p13 chr16: 2,412,367-2,412,367 ABCA17P
    nsv5972718insertion1nstd209human GRCh38 chr16: 2,414,374-2,414,374 , GRCh37.p13 chr16: 2,464,375-2,464,375 ABCA17P
    nsv5969401insertion1nstd209human GRCh38 chr16: 2,382,691-2,382,691 , GRCh37.p13 chr16: 2,432,692-2,432,692 ABCA17P
    nsv5937461copy number variation1nstd209human GRCh38 chr16: 2,366,983-2,367,090 , GRCh37.p13 chr16: 2,416,984-2,417,091 ABCA17P
    nsv5711084mobile element insertion2nstd211human GRCh38 chr16: 2,388,161-2,388,161 , GRCh37.p13 chr16: 2,438,162-2,438,162 ABCA17P
    nsv5710607mobile element insertion1nstd211human GRCh38 chr16: 2,403,283-2,403,283 , GRCh37.p13 chr16: 2,453,284-2,453,284 ABCA17P
    nsv5710302mobile element insertion2nstd211human GRCh38 chr16: 2,362,381-2,362,381 , GRCh37.p13 chr16: 2,412,382-2,412,382 ABCA17P
    nsv5703000mobile element insertion1nstd211human GRCh38 chr16: 2,350,495-2,350,495 , GRCh37.p13 chr16: 2,400,496-2,400,496 ABCA17P
    nsv5660840insertion1nstd207human GRCh38 chr16: 2,387,907-2,387,907 , GRCh37.p13 chr16: 2,437,908-2,437,908 ABCA17P
    nsv5656036insertion1nstd207human GRCh38 chr16: 2,362,366-2,362,366 , GRCh37.p13 chr16: 2,412,367-2,412,367 ABCA17P
    nsv5651238insertion1nstd207human GRCh38 chr16: 2,396,231-2,396,231 , GRCh37.p13 chr16: 2,446,232-2,446,232 ABCA17P
    nsv5591485copy number variation1nstd207human GRCh38 chr16: 2,345,482-2,345,659 , GRCh37.p13 chr16: 2,395,483-2,395,660 ABCA17P
    nsv5526774copy number variation1nstd206human GRCh38 chr16: 2,424,007-2,433,596 , GRCh37.p13 chr16: 2,474,008-2,483,597 ABCA17P, CCNF
    nsv5519410copy number variation1nstd206human GRCh38 chr16: 2,356,618-2,358,671 , GRCh37.p13 chr16: 2,406,619-2,408,672 ABCA17P
    nsv5515791copy number variation1nstd206human GRCh38 chr16: 2,413,439-2,413,605 , GRCh37.p13 chr16: 2,463,440-2,463,606 ABCA17P
    nsv5431365mobile element insertion1nstd206human GRCh38 chr16: 2,350,495-2,350,546 , GRCh37.p13 chr16: 2,400,496-2,400,547 ABCA17P
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