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Items: 1 to 20 of 154

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5958018insertion1nstd209human GRCh38 chr2: 6,763,755-6,763,755 , GRCh37.p13 chr2: 6,903,886-6,903,886 LINC00487
    nsv5868350copy number variation1nstd209human GRCh38 chr2: 6,763,706-6,768,981 , GRCh37.p13 chr2: 6,903,837-6,909,112 LINC00487
    nsv5834009copy number variation1nstd209human GRCh38 chr2: 6,763,426-6,769,986 , GRCh37.p13 chr2: 6,903,557-6,910,117 LINC00487
    nsv5833693copy number variation1nstd209human GRCh38 chr2: 6,766,532-6,767,563 , GRCh37.p13 chr2: 6,906,663-6,907,694 LINC00487
    nsv5688552mobile element insertion1nstd211human GRCh38 chr2: 6,736,244-6,736,244 , GRCh37.p13 chr2: 6,876,375-6,876,375 LINC00487
    nsv5447156copy number variation1nstd206human GRCh38 chr2: 6,752,190-6,752,267 , GRCh37.p13 chr2: 6,892,321-6,892,398 LINC00487
    nsv5442748copy number variation1nstd206human GRCh38 chr2: 6,749,522-6,762,611 , GRCh37.p13 chr2: 6,889,653-6,902,742 LINC00487
    nsv5409856mobile element insertion1nstd206human GRCh38 chr2: 6,736,244-6,736,295 , GRCh37.p13 chr2: 6,876,375-6,876,426 LINC00487
    nsv5357594translocation1nstd200human GRCh38 chr2: 6,767,936-6,767,936 , GRCh38 chr2: 6,767,999-6,767,999 , GRCh37.p13 chr2: 6,908,067-6,908,067 , GRCh37.p13 chr2: 6,908,130-6,908,130 LINC00487
    nsv5357584translocation1nstd200human GRCh38 chr2: 6,752,267-6,752,267 , GRCh38 chr2: 6,752,190-6,752,190 , GRCh37.p13 chr2: 6,892,398-6,892,398 , GRCh37.p13 chr2: 6,892,321-6,892,321 LINC00487
    nsv5331640translocation1nstd200human GRCh37 chr2: 6,908,130-6,908,130 , GRCh37 chr2: 6,908,067-6,908,067 , GRCh38.p12 chr2: 6,767,999-6,767,999 , GRCh38.p12 chr2: 6,767,936-6,767,936 LINC00487
    nsv5068227mobile element insertion1nstd203human GRCh38 chr2: 6,763,755-6,763,774 , GRCh37.p13 chr2: 6,903,886-6,903,905 LINC00487
    nsv4892202copy number variation1nstd200human GRCh38 chr2: 6,760,340-6,769,775 , GRCh37.p13 chr2: 6,900,471-6,909,906 LINC00487
    nsv4892201copy number variation1nstd200human GRCh38 chr2: 6,749,522-6,762,611 , GRCh37.p13 chr2: 6,889,653-6,902,742 LINC00487
    nsv4674461copy number variation1nstd102humanUncertain significance GRCh37 chr2: 6,750,679-7,030,957 , GRCh38.p12 chr2: 6,610,547-6,890,826 MIR7515, MIR7515HG, 6 more genes
    nsv4467367mobile element insertion1nstd166human GRCh37.p13 chr2: 6,875,397-6,875,397 , GRCh38.p12 chr2: 6,735,266-6,735,266 LINC00487
    nsv4454966copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,770-7,502,796 , GRCh38.p12 chr2: 12,770-7,362,665 LINC01810, ADI1, 83 more genes
    nsv3909560copy number variation1nstd102humanLikely pathogenic NCBI36 chr2: 4,442,179-7,690,419 , GRCh37 chr2: 4,464,304-7,772,968 , GRCh38 chr2: 4,416,714-7,632,837 SOX11, RNF144A, 36 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
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