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Items: 1 to 20 of 656

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137702copy number variation1nstd102humanPathogenic GRCh37 chr9: 35,059,633-37,660,586 , GRCh38.p12 chr9: 35,059,636-37,660,589 ARHGEF39, LOC105376026, 84 more genes
    nsv5967075insertion1nstd209human GRCh38 chr9: 35,232,177-35,232,177 , GRCh37.p13 chr9: 35,232,174-35,232,174 UNC13B
    nsv5964631insertion1nstd209human GRCh38 chr9: 35,328,642-35,328,642 , GRCh37.p13 chr9: 35,328,639-35,328,639 UNC13B
    nsv5956418insertion1nstd209human GRCh38 chr9: 35,276,810-35,276,810 , GRCh37.p13 chr9: 35,276,807-35,276,807 UNC13B
    nsv5954606insertion1nstd209human GRCh38 chr9: 35,257,370-35,257,370 , GRCh37.p13 chr9: 35,257,367-35,257,367 UNC13B
    nsv5952937insertion1nstd209human GRCh38 chr9: 35,245,162-35,245,162 , GRCh37.p13 chr9: 35,245,159-35,245,159 UNC13B
    nsv5925097copy number variation1nstd209human GRCh38 chr9: 35,364,132-35,364,312 , GRCh37.p13 chr9: 35,364,129-35,364,309 UNC13B
    nsv5916502copy number variation1nstd209human GRCh38 chr9: 35,183,034-35,183,107 , GRCh37.p13 chr9: 35,183,031-35,183,104 UNC13B
    nsv5916201copy number variation1nstd209human GRCh38 chr9: 35,228,468-35,228,567 , GRCh37.p13 chr9: 35,228,465-35,228,564 UNC13B
    nsv5914000copy number variation1nstd209human GRCh38 chr9: 35,170,369-35,174,528 , GRCh37.p13 chr9: 35,170,366-35,174,525 UNC13B
    nsv5861658copy number variation2nstd209human GRCh38 chr9: 35,169,729-35,174,228 , GRCh37.p13 chr9: 35,169,726-35,174,225 UNC13B
    nsv5856704copy number variation1nstd209human GRCh38 chr9: 35,261,155-35,263,958 , GRCh37.p13 chr9: 35,261,152-35,263,955 UNC13B
    nsv5850642copy number variation1nstd209human GRCh38 chr9: 35,226,489-35,228,521 , GRCh37.p13 chr9: 35,226,486-35,228,518 UNC13B
    nsv5847759copy number variation2nstd209human GRCh38 chr9: 35,170,279-35,174,178 , GRCh37.p13 chr9: 35,170,276-35,174,175 UNC13B
    nsv5723612mobile element insertion1nstd211human GRCh38 chr9: 35,165,043-35,165,043 , GRCh37.p13 chr9: 35,165,040-35,165,040 UNC13B
    nsv5716427mobile element insertion2nstd211human GRCh38 chr9: 35,233,952-35,233,952 , GRCh37.p13 chr9: 35,233,949-35,233,949 UNC13B
    nsv5714617mobile element insertion1nstd211human GRCh38 chr9: 35,193,744-35,193,744 , GRCh37.p13 chr9: 35,193,741-35,193,741 UNC13B
    nsv5710844mobile element insertion1nstd211human GRCh38 chr9: 35,391,103-35,391,103 , GRCh37.p13 chr9: 35,391,100-35,391,100 UNC13B
    nsv5710703mobile element insertion2nstd211human GRCh38 chr9: 35,224,698-35,224,698 , GRCh37.p13 chr9: 35,224,695-35,224,695 UNC13B
    nsv5710687mobile element insertion2nstd211human GRCh38 chr9: 35,245,177-35,245,177 , GRCh37.p13 chr9: 35,245,174-35,245,174 UNC13B
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