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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6122442copy number variation1nstd186human GRCh37 chr16: 57,252,635-57,252,944 , GRCh38.p12 chr16: 57,218,723-57,219,032 RSPRY1
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv5945738copy number variation1nstd209human GRCh38 chr16: 57,187,723-57,187,803 , GRCh37.p13 chr16: 57,221,635-57,221,715 RSPRY1
    nsv5707355mobile element insertion1nstd211human GRCh38 chr16: 57,199,928-57,199,928 , GRCh37.p13 chr16: 57,233,840-57,233,840 RSPRY1
    nsv5706221mobile element insertion1nstd211human GRCh38 chr16: 57,211,732-57,211,732 , GRCh37.p13 chr16: 57,245,644-57,245,644 RSPRY1
    nsv5590030copy number variation1nstd207human GRCh38 chr16: 57,218,709-57,219,031 , GRCh37.p13 chr16: 57,252,621-57,252,943 RSPRY1
    nsv5519309copy number variation1nstd206human GRCh38 chr16: 57,218,723-57,219,032 , GRCh37.p13 chr16: 57,252,635-57,252,944 RSPRY1
    nsv5385196mobile element deletion2nstd186human GRCh37 chr16: 57,252,635-57,252,944 , GRCh38.p12 chr16: 57,218,723-57,219,032 RSPRY1
    nsv5365650translocation1nstd200human GRCh38 chr16: 57,238,873-57,238,873 , GRCh38 chr16: 57,231,319-57,231,319 , GRCh37.p13 chr16: 57,265,231-57,265,231 , GRCh37.p13 chr16: 57,272,785-57,272,785 RSPRY1
    nsv5358220translocation1nstd200human GRCh38 chr16: 57,238,875-57,238,875 , GRCh38 chr16: 57,235,228-57,235,228 , GRCh37.p13 chr16: 57,272,787-57,272,787 , GRCh37.p13 chr16: 57,269,140-57,269,140 RSPRY1
    nsv5358219translocation1nstd200human GRCh38 chr16: 57,234,139-57,234,139 , GRCh38 chr16: 57,233,609-57,233,609 , GRCh37.p13 chr16: 57,267,521-57,267,521 , GRCh37.p13 chr16: 57,268,051-57,268,051 RSPRY1
    nsv5358218translocation1nstd200human GRCh38 chr16: 57,204,503-57,204,503 , GRCh38 chr16: 57,186,451-57,186,451 , GRCh37.p13 chr16: 57,220,363-57,220,363 , GRCh37.p13 chr16: 57,238,415-57,238,415 PSME3IP1, RSPRY1
    nsv5301175copy number variation1nstd204human GRCh38.p13 chr16: 56,771,413-57,511,371 , GRCh37.p13 chr16: 56,805,325-57,545,283 , PLLP, 24 more genes
    nsv5266294copy number variation1nstd204human GRCh38.p13 chr16: 57,181,847-57,184,266 , GRCh37.p13 chr16: 57,215,759-57,218,178 RSPRY1, PSME3IP1
    nsv5266215copy number variation1nstd204human GRCh38.p13 chr16: 57,165,113-57,224,449 , GRCh37.p13 chr16: 57,199,025-57,258,361 RSPRY1, PSME3IP1
    nsv5263209copy number variation1nstd204human GRCh38.p13 chr16: 56,771,401-57,423,100 , GRCh37.p13 chr16: 56,805,313-57,457,012 , NUP93, 19 more genes
    nsv5214209mobile element deletion1nstd204human GRCh38.p13 chr16: 57,218,723-57,219,032 , GRCh37.p13 chr16: 57,252,635-57,252,944 RSPRY1
    nsv5184579mobile element insertion1nstd203human GRCh38 chr16: 57,199,928-57,199,928 , GRCh37.p13 chr16: 57,233,840-57,233,840 RSPRY1
    nsv5008375copy number variation1nstd200human GRCh38 chr16: 57,234,321-57,234,371 , GRCh37.p13 chr16: 57,268,233-57,268,283 RSPRY1
    nsv5008374copy number variation1nstd200human GRCh38 chr16: 57,187,726-57,187,804 , GRCh37.p13 chr16: 57,221,638-57,221,716 RSPRY1
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