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Items: 1 to 20 of 3919

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6114528copy number variation1nstd186human GRCh37 chr15: 21,139,723-21,183,082 , GRCh38.p12 chr15: 20,934,394-20,977,753 OR11J2P, LINC01193, 3 more genes
    nsv5935377copy number variation1nstd209human GRCh38 chr15: 20,058,428-21,065,075 , GRCh37.p13 chr15: 20,263,681-21,270,404 , VN1R60P, 33 more genes
    nsv5380974copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,612,840-23,272,733 , GRCh38.p12 chr15: 20,407,587-22,308,242 OR11J2P, LOC105379205, 82 more genes
    nsv5280286copy number variation1nstd204human GRCh38.p13 chr15: 20,956,301-20,971,300 , GRCh37.p13 chr15: 21,161,630-21,176,629 OR11J5P, OR11J2P, 1 more genes
    nsv5279462copy number variation1nstd204human GRCh38.p13 chr15: 20,949,201-20,960,100 , GRCh37.p13 chr15: 21,154,530-21,165,429 OR11J2P, LINC01193
    nsv5278318copy number variation1nstd204human GRCh38.p13 chr15: 20,957,901-20,960,100 , GRCh37.p13 chr15: 21,163,230-21,165,429 OR11J2P, LINC01193
    nsv5277540copy number variation1nstd204human GRCh38.p13 chr15: 20,958,001-20,977,200 , GRCh37.p13 chr15: 21,163,330-21,182,529 OR11J2P, LINC01193, 1 more genes
    nsv5277531copy number variation1nstd204human GRCh38.p13 chr15: 20,952,401-21,037,100 , GRCh37.p13 chr15: 21,157,730-21,242,429 OR11J2P, LINC01193, 3 more genes
    nsv5276129copy number variation1nstd204human GRCh38.p13 chr15: 20,960,501-20,970,100 , GRCh37.p13 chr15: 21,165,830-21,175,429 OR11J5P, OR11J2P, 1 more genes
    nsv5273627copy number variation1nstd204human GRCh38.p13 chr15: 20,961,101-20,966,300 , GRCh37.p13 chr15: 21,166,430-21,171,629 OR11J2P, LINC01193
    nsv5273536copy number variation1nstd204human GRCh38.p13 chr15: 20,961,501-20,962,300 , GRCh37.p13 chr15: 21,166,830-21,167,629 LINC01193, OR11J2P
    nsv5272524copy number variation1nstd204human GRCh38.p13 chr15: 20,956,301-20,976,500 , GRCh37.p13 chr15: 21,161,630-21,181,829 OR11J5P, LINC01193, 1 more genes
    nsv5267888copy number variation1nstd204human GRCh38.p13 chr15: 20,959,501-20,960,100 , GRCh37.p13 chr15: 21,164,830-21,165,429 LINC01193, OR11J2P
    nsv5266047copy number variation1nstd204human GRCh38.p13 chr15: 20,943,501-20,976,500 , GRCh37.p13 chr15: 21,148,830-21,181,829 LINC01193, OR11J2P, 1 more genes
    nsv5260515copy number variation1nstd204human GRCh38.p13 chr15: 20,956,201-20,962,300 , GRCh37.p13 chr15: 21,161,530-21,167,629 LINC01193, OR11J2P
    nsv5005158copy number variation1nstd200human GRCh38 chr15: 20,190,253-21,192,595 , GRCh37.p13 chr15: 20,395,506-21,397,924 , POTEB2, 33 more genes
    nsv4766438inversion1nstd199human GRCh37 chr15: 20,631,756-22,592,301 , GRCh38.p12 chr15: 20,426,503-22,304,350 , NBEAP1, 87 more genes
    nsv4764432inversion1nstd199human GRCh37 chr15: 20,634,164-22,589,896 , GRCh38.p12 chr15: 20,428,911-22,301,945 , NBEAP1, 87 more genes
    nsv4760900inversion1nstd199human GRCh37 chr15: 20,628,611-22,595,458 , GRCh38.p12 chr15: 20,423,358-22,307,507 , NBEAP1, 87 more genes
    nsv4757759inversion1nstd199human GRCh37 chr15: 20,444,123-21,242,628 , GRCh38.p12 chr15: 20,238,870-21,037,299 , NBEAP1, 28 more genes
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