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Items: 1 to 20 of 175

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5962582insertion1nstd209human GRCh38 chr2: 7,976,936-7,976,936 , GRCh37.p13 chr2: 8,117,067-8,117,067 LINC00298
    nsv5619554insertion1nstd207human GRCh38 chr2: 7,976,936-7,976,936 , GRCh37.p13 chr2: 8,117,067-8,117,067 LINC00298
    nsv5551910insertion1nstd206human GRCh38 chr2: 7,920,912-7,920,962 , GRCh37.p13 chr2: 8,061,043-8,061,093 LINC00298
    nsv5448850copy number variation1nstd206human GRCh38 chr2: 7,937,874-7,937,931 , GRCh37.p13 chr2: 8,078,005-8,078,062 LINC00298
    nsv5439307copy number variation1nstd206human GRCh38 chr2: 7,924,782-7,924,833 , GRCh37.p13 chr2: 8,064,913-8,064,964 LINC00298
    nsv4892241copy number variation1nstd200human GRCh38 chr2: 7,951,975-7,962,220 , GRCh37.p13 chr2: 8,092,106-8,102,351 LINC00298
    nsv4770108copy number variation1nstd200human GRCh37 chr2: 8,077,292-8,077,580 , GRCh38.p12 chr2: 7,937,161-7,937,449 LINC00298
    nsv4769004insertion1nstd186human GRCh37 chr2: 8,117,068-8,117,068 , GRCh38.p12 chr2: 7,976,937-7,976,937 LINC00298
    nsv4763433insertion1nstd199human GRCh37 chr2: 8,117,068-8,117,068 , GRCh38.p12 chr2: 7,976,937-7,976,937 LINC00298
    nsv4723077insertion1nstd186human GRCh37 chr2: 8,117,067-8,117,067 , GRCh38.p12 chr2: 7,976,936-7,976,936 LINC00298
    nsv4684595insertion1nstd194human GRCh37 chr2: 8,117,068-8,117,068 , GRCh38.p12 chr2: 7,976,937-7,976,937 LINC00298
    nsv4673957copy number variation1nstd102humanLikely benign GRCh37 chr2: 7,171,363-8,647,212 , GRCh38.p12 chr2: 7,031,232-8,507,082 LINC00299, LOC101929551, 17 more genes
    nsv4564312mobile element insertion1nstd166human GRCh37.p13 chr2: 8,097,874-8,097,874 , GRCh38.p12 chr2: 7,957,743-7,957,743 LINC00298
    nsv4558409mobile element insertion1nstd166human GRCh37.p13 chr2: 8,079,243-8,079,243 , GRCh38.p12 chr2: 7,939,112-7,939,112 LINC00298
    nsv4536325insertion1nstd166human GRCh37.p13 chr2: 8,117,067-8,117,067 , GRCh38.p12 chr2: 7,976,936-7,976,936 LINC00298
    nsv4467093mobile element insertion1nstd166human GRCh37.p13 chr2: 8,093,303-8,093,303 , GRCh38.p12 chr2: 7,953,172-7,953,172 LINC00298
    nsv4453182copy number variation1nstd102humanUncertain significance GRCh37 chr2: 7,881,175-8,464,031 , GRCh38.p12 chr2: 7,741,044-8,323,901 LINC00298, LOC105373408, 4 more genes
    nsv3908896copy number variation1nstd102humanPathogenic GRCh37 chr2: 6,671,304-16,243,921 , GRCh38 chr2: 6,531,172-16,103,799 , NCBI36 chr2: 6,588,755-16,161,372 RNU6-1288P, MIR7515HG, 138 more genes
    nsv3908628copy number variation1nstd102humanPathogenic NCBI36 chr2: 20,342-14,924,526 , GRCh37 chr2: 30,342-15,007,075 , GRCh38 chr2: 30,342-14,866,951 RPS7, RPL30P3, 198 more genes
    nsv3908605copy number variation1nstd102humanPathogenic GRCh37 chr2: 66,097-55,797,773 , GRCh38 chr2: 66,097-55,570,637 , NCBI36 chr2: 56,097-55,651,277 SLC35F6, LOC105374458, 801 more genes
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