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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5925767copy number variation1nstd209human GRCh38 chr11: 46,757,695-46,757,994 , GRCh37.p13 chr11: 46,779,245-46,779,544 CKAP5
    nsv5856706copy number variation1nstd209human GRCh38 chr11: 46,775,115-46,776,214 , GRCh37.p13 chr11: 46,796,665-46,797,764 CKAP5
    nsv5725968mobile element insertion1nstd211human GRCh38 chr11: 46,822,977-46,822,977 , GRCh37.p13 chr11: 46,844,528-46,844,528 CKAP5
    nsv5702809mobile element insertion2nstd211human GRCh38 chr11: 46,754,591-46,754,591 , GRCh37.p13 chr11: 46,776,141-46,776,141 CKAP5
    nsv5512954copy number variation1nstd206human GRCh38 chr11: 46,752,500-46,757,500 , GRCh37.p13 chr11: 46,774,050-46,779,050 CKAP5, MIR5582
    nsv5496414copy number variation1nstd206human GRCh38 chr11: 46,814,127-46,814,207 , GRCh37.p13 chr11: 46,835,677-46,835,757 CKAP5
    nsv5397372mobile element insertion1nstd206human GRCh38 chr11: 46,754,591-46,754,642 , GRCh37.p13 chr11: 46,776,141-46,776,192 CKAP5
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5380725copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr11: 45,827,353-47,804,770 , GRCh38.p12 chr11: 45,805,802-47,783,218 MIR4688, LOC112268075, 58 more genes
    nsv5373555translocation1nstd200human GRCh38 chr20: 62,945,631-62,945,631 , GRCh38 chr11: 46,838,341-46,838,341 , GRCh37.p13 chr11: 46,859,892-46,859,892 , GRCh37.p13 chr20: 61,576,983-61,576,983 GID8, CKAP5
    nsv5355061translocation1nstd200human GRCh38 chr11: 46,814,207-46,814,207 , GRCh38 chr11: 46,814,127-46,814,127 , GRCh37.p13 chr11: 46,835,677-46,835,677 , GRCh37.p13 chr11: 46,835,757-46,835,757 CKAP5
    nsv5355060translocation1nstd200human GRCh38 chr11: 46,801,482-46,801,482 , GRCh38 chr11: 46,801,560-46,801,560 , GRCh37.p13 chr11: 46,823,032-46,823,032 , GRCh37.p13 chr11: 46,823,110-46,823,110 CKAP5
    nsv5355042translocation1nstd200human GRCh38 chr11: 44,567,534-44,567,534 , GRCh38 chr11: 46,753,331-46,753,331 , GRCh37.p13 chr11: 44,589,084-44,589,084 , GRCh37.p13 chr11: 46,774,881-46,774,881 CD82, CKAP5, 1 more genes
    nsv5339652translocation1nstd200human GRCh37 chr11: 46,823,032-46,823,032 , GRCh37 chr11: 46,823,110-46,823,110 , GRCh38.p12 chr11: 46,801,482-46,801,482 , GRCh38.p12 chr11: 46,801,560-46,801,560 CKAP5
    nsv5335836translocation1nstd200human GRCh37 chr11: 46,774,881-46,774,881 , GRCh37 chr11: 44,589,084-44,589,084 , GRCh38.p12 chr11: 44,567,534-44,567,534 , GRCh38.p12 chr11: 46,753,331-46,753,331 CD82, CKAP5, 1 more genes
    nsv5322374translocation1nstd204human GRCh37.p13 chr11: 44,589,084-44,589,084 , GRCh37.p13 chr11: 46,774,881-46,774,881 , GRCh38.p13 chr11: 44,567,534-44,567,534 , GRCh38.p13 chr11: 46,753,331-46,753,331 CD82, CKAP5, 1 more genes
    nsv5300440copy number variation1nstd204human GRCh38.p13 chr11: 46,755,460-46,757,794 , GRCh37.p13 chr11: 46,777,010-46,779,344 CKAP5
    nsv5279251copy number variation1nstd204human GRCh38.p13 chr11: 46,753,569-46,756,718 , GRCh37.p13 chr11: 46,775,119-46,778,268 MIR5582, CKAP5
    nsv5268020copy number variation1nstd204human GRCh38.p13 chr11: 46,755,419-46,757,793 , GRCh37.p13 chr11: 46,776,969-46,779,343 CKAP5
    nsv5194264mobile element insertion1nstd203human GRCh38 chr11: 46,787,540-46,787,554 , GRCh37.p13 chr11: 46,809,090-46,809,104 CKAP5
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