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Items: 1 to 20 of 621

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    nsv6642688copy number variation1nstd229human GRCh38 chr1: 154,149,454-154,152,039 , GRCh37.p13 chr1: 154,121,930-154,124,515 NUP210L
    nsv6642469copy number variation1nstd229human GRCh38 chr1: 154,108,435-154,112,195 , GRCh37.p13 chr1: 154,080,911-154,084,671 NUP210L
    nsv6642461copy number variation1nstd229human GRCh38 chr1: 154,036,035-154,036,068 , GRCh37.p13 chr1: 154,008,511-154,008,544 NUP210L
    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
    nsv6642342copy number variation1nstd229human GRCh38 chr1: 154,113,063-154,114,207 , GRCh37.p13 chr1: 154,085,539-154,086,683 NUP210L
    nsv6642011copy number variation1nstd229human GRCh38 chr1: 154,107,201-154,109,100 , GRCh37.p13 chr1: 154,079,677-154,081,576 NUP210L
    nsv6549757inversion1nstd223human GRCh38 chr1: 154,013,439-154,013,903 , GRCh37.p13 chr1: 153,985,915-153,986,379 NUP210L
    nsv6549529inversion1nstd223human GRCh38 chr1: 154,076,122-154,077,700 , GRCh37.p13 chr1: 154,048,598-154,050,176 NUP210L, RPS7P2
    nsv6546183inversion1nstd223human GRCh38 chr1: 154,127,860-154,128,569 , GRCh37.p13 chr1: 154,100,336-154,101,045 NUP210L
    nsv6545539inversion1nstd223human GRCh38 chr1: 154,147,859-154,148,226 , GRCh37.p13 chr1: 154,120,335-154,120,702 NUP210L
    nsv6543829inversion1nstd223human GRCh38 chr1: 154,013,534-154,013,795 , GRCh37.p13 chr1: 153,986,010-153,986,271 NUP210L
    nsv6542954inversion1nstd223human GRCh38 chr1: 154,017,288-154,017,535 , GRCh37.p13 chr1: 153,989,764-153,990,011 NUP210L
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