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Items: 1 to 20 of 166

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974643inversion1nstd209human GRCh38 chr9: 133,204,664-133,317,417 , GRCh37.p13 chr9: 136,080,051-136,184,252 , GRCh37.p13 chr9|NW_003315925.1: 30,610-143,511 ABO, OBP2B, 2 more genes
    nsv5924087copy number variation1nstd209human GRCh38 chr9: 133,223,553-133,223,624 , GRCh37.p13 chr9|NW_003315925.1: 49,499-49,570 , GRCh37.p13 chr9: 136,098,940-136,099,011 OBP2B, LCN1P1
    nsv5865549copy number variation1nstd209human GRCh38 chr9: 133,217,241-133,227,029 , GRCh37.p13 chr9: 136,092,628-136,102,416 , GRCh37.p13 chr9|NW_003315925.1: 43,187-52,975 OBP2B, LCN1P1
    nsv5863094copy number variation1nstd209human GRCh38 chr9: 133,220,711-133,224,776 , GRCh37.p13 chr9|NW_003315925.1: 46,657-50,722 , GRCh37.p13 chr9: 136,096,098-136,100,163 LCN1P1, OBP2B
    nsv5861134copy number variation1nstd209human GRCh38 chr9: 133,221,975-133,224,876 , GRCh37.p13 chr9|NW_003315925.1: 47,921-50,822 , GRCh37.p13 chr9: 136,097,362-136,100,263 LCN1P1, OBP2B
    nsv5860843copy number variation1nstd209human GRCh38 chr9: 133,227,080-133,235,646 , GRCh37.p13 chr9: 136,102,467-136,111,033 , GRCh37.p13 chr9|NW_003315925.1: 53,026-61,592 LCN1P1
    nsv5854430copy number variation1nstd209human GRCh38 chr9: 133,224,256-133,232,409 , GRCh37.p13 chr9|NW_003315925.1: 50,202-58,355 , GRCh37.p13 chr9: 136,099,643-136,107,796 LCN1P1
    nsv5133651mobile element insertion1nstd203human GRCh38 chr9: 133,224,938-133,224,943 , GRCh37.p13 chr9|NW_003315925.1: 50,884-50,889 , GRCh37.p13 chr9: 136,100,325-136,100,330 LCN1P1
    nsv4683889copy number variation1nstd102humanUncertain significance GRCh37 chr9: 135,771,850-137,038,881 , GRCh38.p12 chr9: 132,896,463-134,173,759 GBGT1, CELP, 46 more genes
    nsv4681357copy number variation1nstd102humanUncertain significance GRCh37 chr9: 135,771,602-136,769,889 , GRCh38.p12 chr9: 132,896,215-133,904,767 ABO, GTF3C5, 40 more genes
    nsv4675513copy number variation1nstd102humanUncertain significance GRCh37 chr9: 135,920,220-136,139,686 , GRCh38.p12 chr9: 133,044,833-133,264,283 CELP, GTF3C5, 7 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
    nsv4453311copy number variation1nstd102humanUncertain significance GRCh37 chr9: 134,379,574-138,678,377 , GRCh38.p12 chr9: 131,504,187-135,786,531 RNU6ATAC, RPL21P81, 114 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
    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
    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
    nsv3919948copy number variation1nstd102humanPathogenic GRCh37 chr9: 125,554,937-141,018,984 , GRCh38 chr9: 122,792,658-138,124,532 , NCBI36 chr9: 124,594,758-140,138,805 LOC107987143, ATP6V1G1P3, 456 more genes
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