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Items: 1 to 20 of 147

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095753copy number variation1nstd102humanPathogenic GRCh37 chr1: 153,782,653-153,964,569 , GRCh38.p12 chr1: 153,810,177-153,992,093 JTB, LOC101928059, 10 more genes
    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
    nsv7038754inversion1nstd229human GRCh38 chr1: 153,981,649-154,054,681 , GRCh37.p13 chr1: 153,954,125-154,027,157 RAB13, RPS27, 3 more genes
    nsv6642468copy number variation1nstd229human GRCh38 chr1: 153,988,398-153,989,387 , GRCh37.p13 chr1: 153,960,874-153,961,863 RAB13, RPS27
    nsv6642437copy number variation1nstd229human GRCh38 chr1: 153,574,701-154,062,600 , GRCh37.p13 chr1: 153,547,177-154,035,076 S100A13, S100A16, 27 more genes
    nsv6328538copy number variation1nstd223human GRCh38 chr1: 153,953,287-154,092,148 , GRCh37.p13 chr1: 153,925,763-154,064,624 NUP210L, CRTC2, 9 more genes
    nsv6316956copy number variation1nstd223human GRCh38 chr1: 153,988,289-153,989,303 , GRCh37.p13 chr1: 153,960,765-153,961,779 RPS27, RAB13
    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
    nsv6299706copy number variation1nstd186human GRCh37 chr1: 153,961,701-153,962,018 , GRCh38.p12 chr1: 153,989,225-153,989,542 RPS27, RAB13
    nsv6133926copy number variation1nstd213human GRCh37 chr1: 153,540,000-154,010,001 , GRCh38.p12 chr1: 153,567,524-154,037,525 SNAPIN, LOC645965, 26 more genes
    nsv6133737copy number variation1nstd213human GRCh37 chr1: 153,820,000-155,320,001 , GRCh38.p12 chr1: 153,847,524-155,350,210 GBA1LP, PKLR, 81 more genes
    nsv6133734copy number variation1nstd213human GRCh37 chr1: 150,350,000-154,440,001 , GRCh38.p12 chr1: 150,377,524-154,467,525 , MCL1, 216 more genes
    nsv6133560copy number variation1nstd213human GRCh37 chr1: 153,460,000-155,250,001 , GRCh38.p12 chr1: 153,487,524-155,280,210 CKS1B, ILF2, 97 more genes
    nsv6118725copy number variation1nstd186human GRCh37 chr1: 153,960,827-153,961,783 , GRCh38.p12 chr1: 153,988,351-153,989,307 RAB13, RPS27
    nsv5873752copy number variation1nstd209human GRCh38 chr1: 153,988,351-153,989,306 , GRCh37.p13 chr1: 153,960,827-153,961,782 RPS27, RAB13
    nsv5570989copy number variation1nstd207human GRCh38 chr1: 153,988,351-153,989,306 , GRCh37.p13 chr1: 153,960,827-153,961,782 RPS27, RAB13
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