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Items: 1 to 20 of 157

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5863631copy number variation1nstd209human GRCh38 chr9: 128,300,891-128,304,140 , GRCh37.p13 chr9: 131,063,170-131,066,419 TRUB2
    nsv5323246translocation1nstd204human GRCh38.p13 chr9: 128,302,399-128,302,399 , GRCh38.p13 chr9: 128,310,573-128,310,573 , GRCh37.p13 chr9: 131,072,852-131,072,852 , GRCh37.p13 chr9: 131,064,678-131,064,678 TRUB2
    nsv5304184copy number variation1nstd204human GRCh38.p13 chr9: 128,305,668-128,306,698 , GRCh37.p13 chr9: 131,067,947-131,068,977 TRUB2
    nsv5259114copy number variation1nstd204human GRCh38.p13 chr9: 128,307,791-128,310,392 , GRCh37.p13 chr9: 131,070,070-131,072,671 TRUB2
    nsv4988385copy number variation1nstd200human GRCh38 chr9: 128,305,677-128,306,692 , GRCh37.p13 chr9: 131,067,956-131,068,971 TRUB2
    nsv4985740copy number variation1nstd200human GRCh38 chr9: 128,105,845-128,709,294 , GRCh37.p13 chr9: 130,868,124-131,471,573 , SET, 33 more genes
    nsv4834492copy number variation1nstd200human GRCh37 chr9: 131,067,956-131,068,970 , GRCh38.p12 chr9: 128,305,677-128,306,691 TRUB2
    nsv4834307copy number variation1nstd200human GRCh37 chr9: 131,070,732-131,071,124 , GRCh38.p12 chr9: 128,308,453-128,308,845 TRUB2
    nsv4768374copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,412,438-131,423,964 , GRCh38.p12 chr9: 127,650,159-128,661,685 COQ4, GLE1, 53 more genes
    nsv4683557copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,577,951-131,303,459 , GRCh38.p12 chr9: 127,815,672-128,541,180 SWI5, LOC105379841, 36 more genes
    nsv4675731copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,957,344-132,310,210 , GRCh38.p12 chr9: 128,195,065-129,547,931 PTPA, GLE1, 55 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
    nsv4450425copy number variation2nstd102humanPathogenic GRCh37 chr9: 130,374,663-131,329,276 , GRCh38 chr9: 127,612,384-128,566,997 RNU7-171P, MIR2861, 50 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
    nsv4183418copy number variation1nstd166human GRCh37.p13 chr9: 131,067,957-131,068,992 , GRCh38.p12 chr9: 128,305,678-128,306,713 TRUB2
    nsv3924593copy number variation1nstd102humanPathogenic NCBI36 chr9: 130,038,447-130,714,167 , GRCh38 chr9: 128,236,347-128,912,067 , GRCh37 chr9: 130,998,626-131,674,346 LRRC8A, SPOUT1, 34 more genes
    nsv3924370copy number variation1nstd102humanPathogenic NCBI36 chr9: 126,857,965-130,440,046 , GRCh38 chr9: 125,055,865-128,637,946 , GRCh37 chr9: 127,818,144-131,400,225 MVB12B, MIR4672, 97 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
    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
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