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Items: 1 to 20 of 103

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7052094inversion1nstd229human GRCh38 chr3: 132,609,279-139,052,095 , GRCh37.p13 chr3: 132,328,123-138,770,937 RNU6-789P, UBA5, 98 more genes
    nsv7044513inversion1nstd229human GRCh38 chr3: 131,210,998-138,882,695 , GRCh37.p13 chr3: 130,929,842-138,601,537 HSPA8P9, RNU6-1174P, 114 more genes
    nsv7039302inversion1nstd229human GRCh38 chr3: 133,378,933-139,551,784 , GRCh37.p13 chr3: 133,097,777-139,270,626 ESYT3, DONSONP1, 99 more genes
    nsv6727876copy number variation1nstd229human GRCh38 chr3: 133,699,476-133,704,774 , GRCh37.p13 chr3: 133,418,320-133,423,618 INHCAP, TF
    nsv6721762copy number variation1nstd229human GRCh38 chr3: 133,699,501-133,704,700 , GRCh37.p13 chr3: 133,418,345-133,423,544 INHCAP, TF
    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
    nsv6359277copy number variation1nstd223human GRCh38 chr3: 133,708,735-133,711,304 , GRCh37.p13 chr3: 133,427,579-133,430,148 INHCAP, RNA5SP140, 1 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
    nsv6134784copy number variation1nstd213human GRCh37 chr3: 133,070,000-134,020,001 , GRCh38.p12 chr3: 133,351,156-134,301,159 RYK, SLCO2A1, 19 more genes
    nsv6134494copy number variation1nstd213human GRCh37 chr3: 133,330,000-133,510,001 , GRCh38.p12 chr3: 133,611,156-133,791,157 TF, TOPBP1, 6 more genes
    nsv6112714copy number variation1nstd102humanPathogenic GRCh37 chr3: 127,927,712-136,889,323 , GRCh38.p12 chr3: 128,208,869-137,170,481 RNU6-789P, FAM86HP, 169 more genes
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4327115inversion1nstd166human GRCh37.p13 chr3: 131,882,701-162,233,318 , GRCh38.p12 chr3: 132,163,857-162,515,530 , ATP1B3, 446 more genes
    nsv4094832copy number variation1nstd166human GRCh37.p13 chr3: 133,420,519-133,420,635 , GRCh38.p12 chr3: 133,701,675-133,701,791 TF, INHCAP
    nsv3922717copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168 OR7E53P, HSPA8P9, 794 more genes
    nsv3921297copy number variation1nstd102humanPathogenic NCBI36 chr3: 133,918,512-145,986,275 , GRCh38 chr3: 132,716,978-144,784,743 , GRCh37 chr3: 132,435,822-144,503,585 BFSP2, YWHAQP6, 169 more genes
    nsv3920834copy number variation1nstd102humanUncertain significance NCBI36 chr3: 127,308,312-142,119,621 , GRCh38 chr3: 126,106,779-140,918,089 , GRCh37 chr3: 125,825,622-140,636,931 NCK1-DT, LOC107986126, 271 more genes
    nsv3920279copy number variation1nstd102humanPathogenic GRCh38 chr3: 129,817,243-143,381,624 , GRCh37 chr3: 129,536,086-143,100,466 , NCBI36 chr3: 131,018,776-144,583,156 NPHP3-AS1, RNA5SP142, 218 more genes
    nsv3920044copy number variation1nstd102humanPathogenic GRCh38 chr3: 132,972,567-136,894,498 , GRCh37 chr3: 132,691,411-136,613,340 , NCBI36 chr3: 134,174,101-138,096,030 TOPBP1, LOC105374123, 56 more genes
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