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Items: 1 to 20 of 162

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5912574copy number variation1nstd209human GRCh38 chr9: 129,636,326-129,636,547 , GRCh37.p13 chr9: 132,398,605-132,398,826 NTMT1, ASB6
    nsv5909290copy number variation1nstd209human GRCh38 chr9: 129,642,476-129,643,120 , GRCh37.p13 chr9: 132,404,755-132,405,399 ASB6
    nsv5480308copy number variation1nstd206human GRCh38 chr9: 129,642,484-129,643,121 , GRCh37.p13 chr9: 132,404,763-132,405,400 ASB6
    nsv5250774copy number variation1nstd204human GRCh38.p13 chr9: 129,443,501-129,853,600 , GRCh37.p13 chr9: 132,205,780-132,615,879 ASB6, C9orf50, 12 more genes
    nsv4988462copy number variation1nstd200human GRCh38 chr9: 129,642,484-129,643,121 , GRCh37.p13 chr9: 132,404,763-132,405,400 ASB6
    nsv4836349copy number variation1nstd200human GRCh37 chr9: 132,404,763-132,405,400 , GRCh38.p12 chr9: 129,642,484-129,643,121 ASB6
    nsv4673586copy number variation1nstd186human GRCh37 chr9: 132,404,773-132,405,425 , GRCh38.p12 chr9: 129,642,494-129,643,146 ASB6
    nsv4601500copy number variation1nstd183human GRCh37 chr9: 132,404,773-132,405,425 , GRCh38.p12 chr9: 129,642,494-129,643,146 ASB6
    nsv4526045copy number variation1nstd166human GRCh37.p13 chr9: 132,268,998-132,450,000 , GRCh38.p12 chr9: 129,506,719-129,687,721 NTMT1, PRRX2, 4 more genes
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4456688copy number variation1nstd102humanUncertain significance GRCh37 chr9: 132,183,626-133,431,092 , GRCh38.p12 chr9: 129,421,347-130,555,705 ASB6, GPR107, 22 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4430218copy number variation1nstd174human GRCh37 chr9: 132,404,675-132,405,458 , GRCh38.p12 chr9: 129,642,396-129,643,179 ASB6
    nsv4349353copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 131,670,024-134,514,071 , GRCh38.p12 chr9: 128,907,745-131,638,684 ABL1, ASS1, 69 more genes
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
    nsv4188943copy number variation1nstd166human GRCh37.p13 chr9: 132,381,207-132,732,472 , GRCh38.p12 chr9: 129,618,928-129,970,193 PRRX2-AS1, C9orf50, 11 more genes
    nsv4176798copy number variation1nstd166human GRCh37.p13 chr9: 132,404,763-132,405,400 , GRCh38.p12 chr9: 129,642,484-129,643,121 ASB6
    nsv3970331copy number variation1nstd168human GRCh38 chr9: 129,635,608-129,640,348 , GRCh37.p13 chr9: 132,397,887-132,402,627 ASB6, NTMT1
    nsv3924176copy number variation1nstd102humanUncertain significance NCBI36 chr9: 131,113,749-131,668,476 , GRCh37.p13 chr9: 132,073,928-132,628,655 , GRCh38.p12 chr9: 129,311,649-129,866,376 LOC105376292, PRRX2, 17 more genes
    nsv3923672copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,681,755-132,842,253 , GRCh38 chr9: 127,919,476-130,079,974 , NCBI36 chr9: 129,721,576-131,882,074 PIP5KL1, NTMT1, 80 more genes
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