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Items: 1 to 20 of 232

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140772insertion1nstd232human GRCh37.p13 chr1: 154,558,839-154,558,839 , GRCh38.p12 chr1: 154,586,363-154,586,363 ADAR
    nsv7099235copy number variation1nstd231human GRCh38.p12 chr1: 154,116,919-155,715,830 , GRCh37 chr1: 154,089,395-155,685,621 ADAR, CHRNB2, 80 more genes
    nsv7098977copy number variation1nstd102humanUncertain significance GRCh37 chr1: 154,574,314-154,574,460 , GRCh38 chr1: 154,601,838-154,601,984 ADAR
    nsv7095754copy number variation1nstd102humanUncertain significance GRCh37 chr1: 154,557,262-154,557,840 , GRCh38.p12 chr1: 154,584,786-154,585,364 CHRNB2, ADAR
    nsv7095320copy number variation1nstd102humanPathogenic GRCh37 chr1: 153,963,273-154,580,482 , GRCh38.p12 chr1: 153,990,797-154,608,006 RNU6-239P, ATP8B2, 30 more genes
    nsv7056666inversion1nstd229human GRCh38 chr1: 151,403,323-155,722,147 , GRCh37.p13 chr1: 151,375,799-155,691,938 ILF2, SPRR2C, 219 more genes
    nsv7044458inversion1nstd229human GRCh38 chr1: 150,355,899-155,246,175 , GRCh37.p13 chr1: 150,440,214-155,215,966 LCE2C, MUC1, 254 more genes
    nsv7042502inversion1nstd229human GRCh38 chr1: 150,301,267-155,517,761 , GRCh37.p13 chr1: 150,440,214-155,487,552 LINGO4, CELF3, 268 more genes
    nsv7041246inversion1nstd229human GRCh38 chr1: 153,232,460-155,277,038 , GRCh37.p13 chr1: 153,204,936-155,246,829 INTS3, GBA1LP, 111 more genes
    nsv7041047inversion1nstd229human GRCh38 chr1: 154,596,558-159,585,927 , GRCh37.p13 chr1: 154,569,034-159,555,717 ADAR, SNORA80E, 204 more genes
    nsv6642355copy number variation1nstd229human GRCh38 chr1: 154,614,801-154,622,100 , GRCh37.p13 chr1: 154,587,277-154,594,576 ADAR
    nsv6543122inversion1nstd223human GRCh38 chr1: 154,613,330-154,613,834 , GRCh37.p13 chr1: 154,585,806-154,586,310 ADAR
    nsv6538110inversion1nstd223human GRCh38 chr1: 154,593,092-154,593,916 , GRCh37.p13 chr1: 154,565,568-154,566,392 ADAR
    nsv6331417copy number variation1nstd223human GRCh38 chr1: 154,619,543-154,619,990 , GRCh37.p13 chr1: 154,592,019-154,592,466 ADAR
    nsv6310727copy number variation1nstd102humanPathogenic GRCh37 chr1: 154,422,067-154,580,482 , GRCh38.p12 chr1: 154,449,591-154,608,006 ADAR, CHRNB2, 6 more genes
    nsv6310681copy number variation1nstd102humanUncertain significance GRCh37 chr1: 154,569,261-154,571,081 , GRCh38.p12 chr1: 154,596,785-154,598,605 ADAR
    nsv6310678copy number variation4nstd102humanUncertain significance GRCh37 chr1: 149,895,434-156,851,434 , GRCh38.p12 chr1: 149,923,542-156,881,642 PRPF3, KHDC4, 352 more genes
    nsv6310563copy number variation1nstd102humanUncertain significance GRCh38 chr1: 154,601,853-154,601,999 , GRCh37 chr1: 154,574,329-154,574,475 ADAR
    nsv6310523copy number variation1nstd102humanUncertain significance GRCh37 chr1: 154,141,761-156,851,434 , GRCh38.p12 chr1: 154,169,285-156,881,642 MIR555, CFAP141, 135 more genes
    nsv6166865copy number variation1nstd214human GRCh38 chr1: 154,608,404-154,608,519 , GRCh37.p13 chr1: 154,580,880-154,580,995 ADAR
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