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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143806insertion1nstd232human GRCh37.p13 chr1: 154,180,122-154,180,122 , GRCh38.p12 chr1: 154,207,646-154,207,646 C1orf43
    nsv7143646insertion1nstd232human GRCh37.p13 chr1: 154,185,103-154,185,103 , GRCh38.p12 chr1: 154,212,627-154,212,627 C1orf43
    nsv7141306insertion1nstd232human GRCh37.p13 chr1: 154,192,418-154,192,418 , GRCh38.p12 chr1: 154,219,942-154,219,942 UBAP2L, C1orf43
    nsv7139757copy number variation1nstd232human GRCh37.p13 chr1: 154,184,852-154,184,930 , GRCh38.p12 chr1: 154,212,376-154,212,454 C1orf43
    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
    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
    nsv6642345copy number variation1nstd229human GRCh38 chr1: 154,207,647-154,212,318 , GRCh37.p13 chr1: 154,180,123-154,184,794 C1orf43
    nsv6642344copy number variation1nstd229human GRCh38 chr1: 154,189,695-154,207,176 , GRCh37.p13 chr1: 154,162,171-154,179,652 MIR190B, C1orf43, 2 more genes
    nsv6555523inversion1nstd223human GRCh38 chr1: 154,212,678-154,213,316 , GRCh37.p13 chr1: 154,185,154-154,185,792 C1orf43
    nsv6323873copy number variation1nstd223human GRCh38 chr1: 154,189,695-154,207,176 , GRCh37.p13 chr1: 154,162,171-154,179,652 MIR190B, C1orf43, 2 more genes
    nsv6323868copy number variation1nstd223human GRCh38 chr1: 154,215,109-154,216,052 , GRCh37.p13 chr1: 154,187,585-154,188,528 C1orf43
    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
    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
    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
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