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Items: 1 to 20 of 187

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137075copy number variation1nstd102humanUncertain significance GRCh38 chr15: 44,330,225-44,821,972 , GRCh37.p13 chr15: 44,622,423-45,114,170 PATL2, CTDSPL2, 10 more genes
    nsv7094709copy number variation1nstd102humanPathogenic GRCh37 chr15: 44,855,319-44,952,834 , GRCh38.p12 chr15: 44,563,121-44,660,636 EIF3J, SPG11
    nsv7094536copy number variation1nstd102humanUncertain significance GRCh37 chr15: 44,855,319-44,878,413 , GRCh38.p12 chr15: 44,563,121-44,586,215 EIF3J, SPG11
    nsv7064777inversion1nstd229human GRCh38 chr15: 44,555,398-44,555,411 , GRCh37.p13 chr15: 44,847,596-44,847,609 EIF3J
    nsv7062042inversion1nstd229human GRCh38 chr15: 38,786,391-46,534,887 , GRCh37.p13 chr15: 39,078,592-46,827,085 EHD4-AS1, PLA2G4B, 219 more genes
    nsv6974572copy number variation1nstd229human GRCh38 chr15: 44,558,850-44,587,420 , GRCh37.p13 chr15: 44,851,048-44,879,618 EIF3J, SPG11
    nsv6622897copy number variation1nstd224human GRCh37 chr15: 44,250,911-44,859,744 , GRCh38.p12 chr15: 43,958,713-44,567,546 SPG11, HNRNPMP1, 8 more genes
    nsv6593077inversion1nstd223human GRCh38 chr15: 44,546,857-44,549,417 , GRCh37.p13 chr15: 44,839,055-44,841,615 EIF3J
    nsv6591926inversion1nstd223human GRCh38 chr15: 44,552,298-44,553,504 , GRCh37.p13 chr15: 44,844,496-44,845,702 EIF3J
    nsv6587623inversion1nstd223human GRCh38 chr15: 44,552,422-44,553,176 , GRCh37.p13 chr15: 44,844,620-44,845,374 EIF3J
    nsv6583708inversion1nstd223human GRCh38 chr15: 44,544,099-44,544,703 , GRCh37.p13 chr15: 44,836,297-44,836,901 EIF3J
    nsv6509143copy number variation1nstd223human GRCh38 chr15: 44,539,278-44,539,652 , GRCh37.p13 chr15: 44,831,476-44,831,850 EIF3J
    nsv6498798copy number variation1nstd223human GRCh38 chr15: 44,557,901-44,560,000 , GRCh37.p13 chr15: 44,850,099-44,852,198 EIF3J
    nsv6315295copy number variation1nstd102humanPathogenic GRCh37 chr15: 44,855,500-44,859,621 , GRCh38.p12 chr15: 44,563,302-44,567,423 EIF3J, SPG11
    nsv6314026copy number variation1nstd102humanUncertain significance GRCh37 chr15: 44,346,958-44,853,978 , GRCh38.p12 chr15: 44,054,760-44,561,780 GAPDHP43, GOLM2, 7 more genes
    nsv6309618copy number variation1nstd102humanUncertain significance GRCh37 chr15: 44,855,319-44,867,259 , GRCh38.p12 chr15: 44,563,121-44,575,061 EIF3J, SPG11
    nsv6133147copy number variation1nstd213human GRCh37 chr15: 44,080,000-45,200,001 , GRCh38.p12 chr15: 43,787,802-44,907,803 ACTBP7, EIF3J, 24 more genes
    nsv6035553copy number variation1nstd212human GRCh38 chr15: 44,542,875-44,543,010 , GRCh37.p13 chr15: 44,835,073-44,835,208 EIF3J
    nsv6032594copy number variation1nstd212human GRCh38 chr15: 44,539,125-44,547,526 , GRCh37.p13 chr15: 44,831,323-44,839,724 EIF3J
    nsv6023229copy number variation1nstd212human GRCh38 chr15: 44,364,203-44,857,549 , GRCh37.p13 chr15: 44,656,401-45,149,747 TRIM69, SPG11, 11 more genes
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