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Items: 1 to 20 of 445

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145544insertion1nstd232human GRCh37.p13 chr1: 153,792,213-153,792,213 , GRCh38.p12 chr1: 153,819,737-153,819,737 , GRCh38.p12 chr1|NW_003315905.1: 136,438-136,438 GATAD2B
    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
    nsv7095752copy number variation1nstd102humanUncertain significance GRCh37 chr1: 153,782,653-153,800,823 , GRCh38.p12 chr1: 153,810,177-153,828,347 , GRCh38.p12 chr1|NW_003315905.1: 126,878-145,048 GATAD2B
    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
    nsv7044454inversion1nstd229human GRCh38 chr1: 153,885,929-153,893,480 , GRCh37.p13 chr1: 153,858,405-153,865,956 GATAD2B
    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
    nsv6642466copy number variation1nstd229human GRCh38 chr1: 153,887,864-153,890,626 , GRCh37.p13 chr1: 153,860,340-153,863,102 GATAD2B
    nsv6642465copy number variation1nstd229human GRCh38 chr1: 153,870,396-153,877,705 , GRCh37.p13 chr1: 153,842,872-153,850,181 GATAD2B
    nsv6642464copy number variation1nstd229human GRCh38 chr1: 153,847,580-153,867,815 , GRCh37.p13 chr1: 153,820,056-153,840,291 GATAD2B, LOC645965
    nsv6642456copy number variation1nstd229human GRCh38 chr1: 153,887,901-153,890,600 , GRCh37.p13 chr1: 153,860,377-153,863,076 GATAD2B
    nsv6642455copy number variation1nstd229human GRCh38 chr1: 153,874,025-153,909,426 , GRCh37.p13 chr1: 153,846,501-153,881,902 GATAD2B
    nsv6642454copy number variation1nstd229human GRCh38 chr1: 153,862,797-153,866,844 , GRCh37.p13 chr1: 153,835,273-153,839,320 GATAD2B
    nsv6642453copy number variation1nstd229human GRCh38 chr1: 153,838,917-153,842,372 , GRCh37.p13 chr1: 153,811,393-153,814,848 GATAD2B
    nsv6642452copy number variation1nstd229human GRCh38 chr1: 153,831,706-153,842,055 , GRCh37.p13 chr1: 153,804,182-153,814,531 GATAD2B
    nsv6642444copy number variation1nstd229human GRCh38 chr1: 153,700,801-153,827,400 , GRCh37.p13 chr1: 153,673,277-153,799,876 GATAD2B, LOC343052, 4 more genes
    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
    nsv6642338copy number variation1nstd229human GRCh38 chr1: 153,894,839-153,901,192 , GRCh37.p13 chr1: 153,867,315-153,873,668 GATAD2B
    nsv6642336copy number variation1nstd229human GRCh38 chr1: 153,865,387-153,868,892 , GRCh37.p13 chr1: 153,837,863-153,841,368 GATAD2B
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