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Items: 1 to 20 of 109

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5922400copy number variation1nstd209human GRCh38 chr9: 124,865,057-124,868,033 , GRCh37.p13 chr9: 127,627,336-127,630,312 ARPC5L
    nsv5910954copy number variation1nstd209human GRCh38 chr9: 124,864,870-124,864,960 , GRCh37.p13 chr9: 127,627,149-127,627,239 ARPC5L
    nsv5856323copy number variation1nstd209human GRCh38 chr9: 124,866,587-124,868,286 , GRCh37.p13 chr9: 127,628,866-127,630,565 ARPC5L
    nsv5849673copy number variation1nstd209human GRCh38 chr9: 124,865,387-124,868,086 , GRCh37.p13 chr9: 127,627,666-127,630,365 ARPC5L
    nsv5487604copy number variation1nstd206human GRCh38 chr9: 124,865,845-124,866,460 , GRCh37.p13 chr9: 127,628,124-127,628,739 ARPC5L
    nsv5199975mobile element insertion1nstd203human GRCh38 chr9: 124,863,446-124,863,462 , GRCh37.p13 chr9: 127,625,725-127,625,741 ARPC5L
    nsv5127241mobile element insertion1nstd203human GRCh38 chr9: 124,865,264-124,865,264 , GRCh37.p13 chr9: 127,627,543-127,627,543 ARPC5L
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4835919copy number variation1nstd200human GRCh37 chr9: 127,633,390-127,634,988 , GRCh38.p12 chr9: 124,871,111-124,872,709 ARPC5L
    nsv4607677copy number variation1nstd183human GRCh37 chr9: 127,623,815-127,631,654 , GRCh38.p12 chr9: 124,861,536-124,869,375 RPL35, ARPC5L
    nsv4602651copy number variation1nstd183human GRCh37 chr9: 127,599,161-127,644,882 , GRCh38.p12 chr9: 124,836,882-124,882,603 GOLGA1, RPL35, 2 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
    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
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
    nsv4327919inversion1nstd166human GRCh37.p13 chr9: 127,628,794-127,629,708 , GRCh38.p12 chr9: 124,866,515-124,867,429 ARPC5L
    nsv3922684copy number variation2nstd102humanPathogenic NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897 TDRD7, CDK9, 2170 more genes
    nsv3922263copy number variation1nstd102humanPathogenic NCBI36 chr9: 124,897,698-128,495,943 , GRCh38 chr9: 123,095,598-126,693,843 , GRCh37 chr9: 125,857,877-129,456,122 OLFML2A, LHX2-AS1, 64 more genes
    nsv3921598copy number variation1nstd102humanPathogenic GRCh38 chr9: 203,861-138,125,937 , NCBI36 chr9: 193,861-140,140,210 , GRCh37 chr9: 203,861-141,020,389 PGAP4, ECPAS, 2167 more genes
    nsv3920829copy number variation1nstd102humanPathogenic GRCh38 chr9: 121,112,395-138,075,224 , GRCh37 chr9: 123,874,673-140,969,676 , NCBI36 chr9: 122,914,494-140,089,497 LOC101928786, NRON, 495 more genes
    nsv3920713copy number variation1nstd102humanPathogenic NCBI36 chr9: 193,862-140,140,210 , GRCh38 chr9: 203,862-138,125,937 , GRCh37 chr9: 203,862-141,020,389 ABHD17B, LOC100533707, 2167 more genes
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