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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970404inversion1nstd209human GRCh38 chr5: 174,416,203-174,417,409 , GRCh37.p13 chr5: 173,843,206-173,844,412 LINC01411
    nsv5901718copy number variation1nstd209human GRCh38 chr5: 172,153,284-177,326,767 , GRCh37.p13 chr5: 171,580,288-176,753,768 , LOC107986487, 114 more genes
    nsv5899418copy number variation1nstd209human GRCh38 chr5: 174,487,923-174,487,983 , GRCh37.p13 chr5: 173,914,926-173,914,986 LINC01411
    nsv5895507copy number variation1nstd209human GRCh38 chr5: 174,521,767-174,522,062 , GRCh37.p13 chr5: 173,948,770-173,949,065 LINC01411, LOC105377739
    nsv5888652copy number variation1nstd209human GRCh38 chr5: 174,416,219-174,419,076 , GRCh37.p13 chr5: 173,843,222-173,846,079 LINC01411
    nsv5842198copy number variation1nstd209human GRCh38 chr5: 174,418,572-174,420,552 , GRCh37.p13 chr5: 173,845,575-173,847,555 LINC01411
    nsv5841587copy number variation1nstd209human GRCh38 chr5: 174,416,397-174,419,277 , GRCh37.p13 chr5: 173,843,400-173,846,280 LINC01411
    nsv5689406mobile element insertion1nstd211human GRCh38 chr5: 174,488,160-174,488,160 , GRCh37.p13 chr5: 173,915,163-173,915,163 LINC01411
    nsv5688861mobile element insertion2nstd211human GRCh38 chr5: 174,507,862-174,507,862 , GRCh37.p13 chr5: 173,934,865-173,934,865 LINC01411
    nsv5685794mobile element insertion2nstd211human GRCh38 chr5: 174,486,663-174,486,663 , GRCh37.p13 chr5: 173,913,666-173,913,666 LINC01411
    nsv5678532mobile element insertion1nstd211human GRCh38 chr5: 174,506,049-174,506,049 , GRCh37.p13 chr5: 173,933,052-173,933,052 LINC01411
    nsv5638303insertion1nstd207human GRCh38 chr5: 174,521,839-174,521,839 , GRCh37.p13 chr5: 173,948,842-173,948,842 LINC01411, LOC105377739
    nsv5633098insertion1nstd207human GRCh38 chr5: 174,486,651-174,486,651 , GRCh37.p13 chr5: 173,913,654-173,913,654 LINC01411
    nsv5632322insertion1nstd207human GRCh38 chr5: 174,522,129-174,522,129 , GRCh37.p13 chr5: 173,949,132-173,949,132 LINC01411, LOC105377739
    nsv5627782insertion1nstd207human GRCh38 chr5: 174,522,486-174,522,486 , GRCh37.p13 chr5: 173,949,489-173,949,489 LINC01411, LOC105377739
    nsv5574866copy number variation1nstd207human GRCh38 chr5: 174,521,763-174,521,947 , GRCh37.p13 chr5: 173,948,766-173,948,950 LINC01411, LOC105377739
    nsv5561548sequence alteration1nstd206human GRCh38 chr5: 174,416,205-174,419,108 , GRCh37.p13 chr5: 173,843,208-173,846,111 LINC01411
    nsv5545803insertion1nstd206human GRCh38 chr5: 174,378,296-174,378,318 , GRCh37.p13 chr5: 173,805,299-173,805,321 LINC01411
    nsv5538898insertion1nstd206human GRCh38 chr5: 174,486,663-174,486,699 , GRCh37.p13 chr5: 173,913,666-173,913,702 LINC01411
    nsv5465568copy number variation1nstd206human GRCh38 chr5: 174,407,264-174,408,974 , GRCh37.p13 chr5: 173,834,267-173,835,977 LINC01411
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