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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
    nsv7096531copy number variation1nstd102humanUncertain significance GRCh37 chr3: 121,489,192-125,313,644 , GRCh38.p12 chr3: 121,770,345-125,594,800 MEMO1P6, HACD2, 62 more genes
    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
    nsv6703931copy number variation1nstd229human GRCh38 chr3: 118,573,267-126,079,281 , GRCh37.p13 chr3: 118,292,114-125,798,124 RPS24P9, LOC105374064, 149 more genes
    nsv6703872copy number variation1nstd229human GRCh38 chr3: 122,370,482-122,376,167 , GRCh37.p13 chr3: 122,089,329-122,095,014 MIX23
    nsv6698629copy number variation1nstd229human GRCh38 chr3: 122,363,278-122,363,874 , GRCh37.p13 chr3: 122,082,125-122,082,721 MIX23
    nsv6698407copy number variation1nstd229human GRCh38 chr3: 122,157,201-122,395,100 , GRCh37.p13 chr3: 121,876,048-122,113,947 CSTA, MIX23, 3 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6370959copy number variation1nstd223human GRCh38 chr3: 122,381,201-122,389,000 , GRCh37.p13 chr3: 122,100,048-122,107,847 MIX23, FAM162A
    nsv6361636copy number variation1nstd223human GRCh38 chr3: 122,345,397-122,364,628 , GRCh37.p13 chr3: 122,064,244-122,083,475 MIX23
    nsv6358136copy number variation1nstd223human GRCh38 chr3: 122,370,481-122,376,166 , GRCh37.p13 chr3: 122,089,328-122,095,013 MIX23
    nsv6356127copy number variation1nstd223human GRCh38 chr3: 122,363,278-122,363,874 , GRCh37.p13 chr3: 122,082,125-122,082,721 MIX23
    nsv6315285copy number variation1nstd102humanUncertain significance GRCh38 chr3: 122,157,406-123,113,479 , GRCh37.p13 chr3: 121,876,253-122,832,326 SEMA5B, EIF4BP8, 19 more genes
    nsv6311770copy number variation1nstd102humanPathogenic GRCh37 chr3: 120,365,818-133,465,047 , GRCh38.p12 chr3: 120,646,971-133,746,203 HNRNPA1P23, MIX23, 278 more genes
    nsv6254617mobile element insertion1nstd215human GRCh38 chr3: 122,374,100-122,374,100 , GRCh37.p13 chr3: 122,092,947-122,092,947 MIX23
    nsv6254616mobile element insertion1nstd215human GRCh38 chr3: 122,368,121-122,368,121 , GRCh37.p13 chr3: 122,086,968-122,086,968 MIX23
    nsv6134575copy number variation1nstd213human GRCh37 chr3: 116,870,000-132,100,001 , GRCh38.p12 chr3: 117,151,153-132,381,157 ACP3, ADCY5, 308 more genes
    nsv6112688copy number variation1nstd102humanPathogenic GRCh37 chr3: 120,154,188-128,324,987 , GRCh38.p12 chr3: 120,435,341-128,606,144 RNU4-62P, MTCO1P29, 169 more genes
    nsv5973212inversion1nstd209human GRCh38 chr3: 121,858,185-122,522,926 , GRCh37.p13 chr3: 121,577,032-122,241,773 CASR, CD86, 12 more genes
    nsv5906738copy number variation1nstd209human GRCh38 chr3: 122,363,277-122,363,873 , GRCh37.p13 chr3: 122,082,124-122,082,720 MIX23
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