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Items: 1 to 20 of 174

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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
    nsv7050714inversion1nstd229human GRCh38 chr3: 119,886,071-121,104,541 , GRCh37.p13 chr3: 119,604,918-120,823,388 PARLP1, LOC105374069, 26 more genes
    nsv7041333inversion1nstd229human GRCh38 chr3: 119,602,733-121,708,334 , GRCh37.p13 chr3: 119,321,580-121,427,181 RABL3, PTOV1P1, 44 more genes
    nsv7039920inversion1nstd229human GRCh38 chr3: 119,602,735-121,711,940 , GRCh37.p13 chr3: 119,321,582-121,430,787 LINC02049, GSK3B, 44 more genes
    nsv6716122copy number variation1nstd229human GRCh38 chr3: 120,336,801-120,352,000 , GRCh37.p13 chr3: 120,055,648-120,070,847 BTNL12P, LRRC58
    nsv6712971copy number variation1nstd229human GRCh38 chr3: 120,332,701-120,352,900 , GRCh37.p13 chr3: 120,051,548-120,071,747 BTNL12P, LRRC58
    nsv6711465copy number variation1nstd229human GRCh38 chr3: 120,316,705-120,538,307 , GRCh37.p13 chr3: 120,035,552-120,257,154 LRRC58, FSTL1, 5 more genes
    nsv6710068copy number variation1nstd229human GRCh38 chr3: 120,325,128-120,325,212 , GRCh37.p13 chr3: 120,043,975-120,044,059 LRRC58
    nsv6708958copy number variation1nstd229human GRCh38 chr3: 120,170,942-120,680,421 , GRCh37.p13 chr3: 119,889,789-120,399,268 HGD, LOC105374065, 10 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
    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
    nsv6637150copy number variation1nstd102humanUncertain significance GRCh37 chr3: 116,109,191-120,328,013 , GRCh38.p12 chr3: 116,390,344-120,609,166 LOC101926953, LOC105374058, 60 more genes
    nsv6572643inversion1nstd223human GRCh38 chr3: 120,339,811-120,340,714 , GRCh37.p13 chr3: 120,058,658-120,059,561 LRRC58
    nsv6369954copy number variation1nstd223human GRCh38 chr3: 120,231,645-120,942,998 , GRCh37.p13 chr3: 119,950,492-120,661,845 LOC105374069, BTNL12P, 17 more genes
    nsv6365029copy number variation1nstd223human GRCh38 chr3: 120,336,015-120,336,537 , GRCh37.p13 chr3: 120,054,862-120,055,384 LRRC58
    nsv6364838copy number variation1nstd223human GRCh38 chr3: 120,345,601-120,352,800 , GRCh37.p13 chr3: 120,064,448-120,071,647 LRRC58, BTNL12P
    nsv6313492copy number variation1nstd102humanUncertain significance GRCh37 chr3: 119,844,770-120,822,965 , GRCh38.p12 chr3: 120,125,923-121,104,118 RABL3, PTOV1P1, 20 more genes
    nsv6134576copy number variation1nstd213human GRCh37 chr3: 119,550,000-121,140,001 , GRCh38.p12 chr3: 119,831,153-121,421,154 GSK3B, GTF2E1, 27 more genes
    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
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