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Items: 1 to 20 of 212

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095032copy number variation1nstd102humanPathogenic GRCh37 chr16: 57,242,967-57,243,119 , GRCh38.p12 chr16: 57,209,055-57,209,207 RSPRY1
    nsv7095031copy number variation2nstd102humanPathogenic GRCh37 chr16: 56,226,148-58,768,132 , GRCh38.p12 chr16: 56,192,236-58,734,228 MT1B, LOC105371293, 92 more genes
    nsv7094589copy number variation1nstd102humanPathogenic GRCh37 chr16: 57,016,057-58,768,132 , GRCh38.p12 chr16: 56,982,145-58,734,228 SLC38A7, SETD6, 58 more genes
    nsv7061300inversion1nstd229human GRCh38 chr16: 57,193,070-57,193,771 , GRCh37.p13 chr16: 57,226,982-57,227,683 RSPRY1
    nsv6996936copy number variation1nstd229human GRCh38 chr16: 57,220,640-57,221,026 , GRCh37.p13 chr16: 57,254,552-57,254,938 RSPRY1
    nsv6995708copy number variation1nstd229human GRCh38 chr16: 57,221,462-57,221,591 , GRCh37.p13 chr16: 57,255,374-57,255,503 RSPRY1
    nsv6994637copy number variation1nstd229human GRCh38 chr16: 57,234,801-57,237,200 , GRCh37.p13 chr16: 57,268,713-57,271,112 RSPRY1
    nsv6986991copy number variation1nstd229human GRCh38 chr16: 57,059,649-57,664,041 , GRCh37.p13 chr16: 57,093,561-57,697,953 CPNE2, TRL-CAG2-1, 21 more genes
    nsv6982911copy number variation1nstd229human GRCh38 chr16: 57,218,723-57,219,032 , GRCh37.p13 chr16: 57,252,635-57,252,944 RSPRY1
    nsv6982470copy number variation1nstd229human GRCh38 chr16: 57,187,726-57,187,804 , GRCh37.p13 chr16: 57,221,638-57,221,716 RSPRY1
    nsv6982271copy number variation1nstd229human GRCh38 chr16: 57,197,925-57,197,970 , GRCh37.p13 chr16: 57,231,837-57,231,882 RSPRY1
    nsv6978796copy number variation1nstd229human GRCh38 chr16: 57,188,147-57,195,101 , GRCh37.p13 chr16: 57,222,059-57,229,013 RSPRY1
    nsv6978535copy number variation1nstd229human GRCh38 chr16: 57,188,715-57,538,791 , GRCh37.p13 chr16: 57,222,627-57,572,703 CX3CL1, ARL2BP, 13 more genes
    nsv6637586copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,573-62,203,182 , GRCh38.p12 chr16: 46,469,661-62,169,278 LINC02140, LOC100130602, 279 more genes
    nsv6595265inversion1nstd223human GRCh38 chr16: 57,189,678-57,190,116 , GRCh37.p13 chr16: 57,223,590-57,224,028 RSPRY1
    nsv6587916inversion1nstd223human GRCh38 chr16: 57,206,366-57,206,497 , GRCh37.p13 chr16: 57,240,278-57,240,409 RSPRY1
    nsv6587338inversion1nstd223human GRCh38 chr16: 57,209,968-57,210,744 , GRCh37.p13 chr16: 57,243,880-57,244,656 RSPRY1
    nsv6584354inversion1nstd223human GRCh38 chr16: 57,236,869-57,237,460 , GRCh37.p13 chr16: 57,270,781-57,271,372 RSPRY1
    nsv6579411inversion1nstd223human GRCh38 chr16: 57,206,420-57,206,573 , GRCh37.p13 chr16: 57,240,332-57,240,485 RSPRY1
    nsv6501847copy number variation1nstd223human GRCh38 chr16: 57,209,886-57,211,791 , GRCh37.p13 chr16: 57,243,798-57,245,703 RSPRY1
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