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Items: 1 to 20 of 377

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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
    nsv6737359copy number variation1nstd229human GRCh38 chr3: 133,796,828-133,797,583 , GRCh37.p13 chr3: 133,515,672-133,516,427 SRPRB, LOC105374116, 1 more genes
    nsv6733663copy number variation1nstd229human GRCh38 chr3: 133,695,844-133,696,034 , GRCh37.p13 chr3: 133,414,688-133,414,878 TF
    nsv6727876copy number variation1nstd229human GRCh38 chr3: 133,699,476-133,704,774 , GRCh37.p13 chr3: 133,418,320-133,423,618 INHCAP, TF
    nsv6726893copy number variation1nstd229human GRCh38 chr3: 133,745,601-133,747,200 , GRCh37.p13 chr3: 133,464,445-133,466,044 TF
    nsv6724951copy number variation1nstd229human GRCh38 chr3: 133,784,647-133,813,293 , GRCh37.p13 chr3: 133,503,491-133,532,137 SRPRB, LOC105374116, 1 more genes
    nsv6721762copy number variation1nstd229human GRCh38 chr3: 133,699,501-133,704,700 , GRCh37.p13 chr3: 133,418,345-133,423,544 INHCAP, TF
    nsv6721263copy number variation1nstd229human GRCh38 chr3: 133,670,520-133,682,063 , GRCh37.p13 chr3: 133,389,364-133,400,907 TF
    nsv6719211copy number variation1nstd229human GRCh38 chr3: 133,733,556-133,740,820 , GRCh37.p13 chr3: 133,452,400-133,459,664 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
    nsv6564803inversion1nstd223human GRCh38 chr3: 133,665,662-133,666,171 , GRCh37.p13 chr3: 133,384,506-133,385,015 TF
    nsv6560072inversion1nstd223human GRCh38 chr3: 133,679,397-133,679,484 , GRCh37.p13 chr3: 133,398,241-133,398,328 TF
    nsv6369053copy number variation1nstd223human GRCh38 chr3: 133,670,520-133,682,059 , GRCh37.p13 chr3: 133,389,364-133,400,903 TF
    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
    nsv6262975copy number variation1nstd214human GRCh38 chr3: 133,740,916-133,740,985 , GRCh37.p13 chr3: 133,459,760-133,459,829 TF
    nsv6254696mobile element insertion1nstd215human GRCh38 chr3: 133,750,774-133,750,774 , GRCh37.p13 chr3: 133,469,618-133,469,618 TF
    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
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