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Items: 1 to 20 of 441

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148201copy number variation1nstd102humanPathogenic GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857 NECTIN3, H2BP3, 418 more genes
    nsv7098849copy number variation1nstd102humanPathogenic GRCh37 chr3: 110,943,783-115,859,912 , GRCh38.p12 chr3: 111,224,936-116,141,065 ATG3, SIDT1, 81 more genes
    nsv7051524inversion1nstd229human GRCh38 chr3: 110,492,556-118,654,181 , GRCh37.p13 chr3: 110,211,403-118,373,028 MIR8076, ZBTB20-AS4, 106 more genes
    nsv7049104inversion1nstd229human GRCh38 chr3: 114,751,914-119,661,867 , GRCh37.p13 chr3: 114,470,761-119,380,714 LINC00901, EIF4E2P2, 50 more genes
    nsv7038526inversion1nstd229human GRCh38 chr3: 115,622,738-115,622,762 , GRCh37.p13 chr3: 115,341,585-115,341,609 GAP43
    nsv6713799copy number variation1nstd229human GRCh38 chr3: 115,531,601-115,650,800 , GRCh37.p13 chr3: 115,250,448-115,369,647 GAP43
    nsv6712573copy number variation1nstd229human GRCh38 chr3: 115,660,299-115,665,700 , GRCh37.p13 chr3: 115,379,146-115,384,547 GAP43
    nsv6711642copy number variation1nstd229human GRCh38 chr3: 115,717,713-115,737,536 , GRCh37.p13 chr3: 115,436,560-115,456,383 GAP43
    nsv6710679copy number variation1nstd229human GRCh38 chr3: 115,686,640-115,710,182 , GRCh37.p13 chr3: 115,405,487-115,429,029 GAP43
    nsv6710568copy number variation1nstd229human GRCh38 chr3: 115,706,153-115,706,813 , GRCh37.p13 chr3: 115,425,000-115,425,660 GAP43
    nsv6709240copy number variation1nstd229human GRCh38 chr3: 115,692,340-115,699,755 , GRCh37.p13 chr3: 115,411,187-115,418,602 GAP43
    nsv6707907copy number variation1nstd229human GRCh38 chr3: 113,856,250-122,791,940 , GRCh37.p13 chr3: 113,575,097-122,510,787 COX17, LOC105374052, 133 more genes
    nsv6707307copy number variation1nstd229human GRCh38 chr3: 115,635,701-115,638,000 , GRCh37.p13 chr3: 115,354,548-115,356,847 GAP43
    nsv6706183copy number variation1nstd229human GRCh38 chr3: 115,665,705-115,671,201 , GRCh37.p13 chr3: 115,384,552-115,390,048 GAP43
    nsv6705829copy number variation1nstd229human GRCh38 chr3: 115,642,253-115,642,965 , GRCh37.p13 chr3: 115,361,100-115,361,812 GAP43
    nsv6700051copy number variation1nstd229human GRCh38 chr3: 115,640,155-115,650,975 , GRCh37.p13 chr3: 115,359,002-115,369,822 GAP43
    nsv6636198copy number variation1nstd102humanUncertain significance GRCh37 chr3: 115,364,084-115,667,101 , GRCh38.p12 chr3: 115,645,237-115,948,254 GAP43, LOC105374053, 3 more genes
    nsv6628628copy number variation1nstd224human GRCh37 chr3: 115,219,766-115,869,444 , GRCh38.p12 chr3: 115,500,919-116,150,597 GAP43, LSAMP, 4 more genes
    nsv6558695inversion1nstd223human GRCh38 chr3: 115,305,653-119,971,699 , GRCh37.p13 chr3: 115,024,500-119,690,546 LOC105374060, RN7SL815P, 52 more genes
    nsv6558026inversion1nstd223human GRCh38 chr3: 115,668,477-115,669,063 , GRCh37.p13 chr3: 115,387,324-115,387,910 GAP43
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