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Items: 1 to 20 of 252

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144415copy number variation1nstd232human GRCh37.p13 chr3: 133,686,652-133,686,751 , GRCh38.p12 chr3: 133,967,808-133,967,907 SLCO2A1
    nsv7096933copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 133,661,429-133,698,482 , GRCh38.p12 chr3: 133,942,585-133,979,638 SLCO2A1
    nsv7096694copy number variation1nstd102humanUncertain significance GRCh37 chr3: 133,653,557-133,674,057 , GRCh38.p12 chr3: 133,934,713-133,955,213 SLCO2A1
    nsv7054084inversion1nstd229human GRCh38 chr3: 133,945,466-134,167,023 , GRCh37.p13 chr3: 133,664,310-133,885,867 LOC105374117, SLCO2A1, 2 more genes
    nsv7052094inversion1nstd229human GRCh38 chr3: 132,609,279-139,052,095 , GRCh37.p13 chr3: 132,328,123-138,770,937 RNU6-789P, UBA5, 98 more genes
    nsv7048686inversion1nstd229human GRCh38 chr3: 133,888,140-134,120,089 , GRCh37.p13 chr3: 133,606,984-133,838,933 LOC105374117, SLCO2A1, 3 more genes
    nsv7048113inversion1nstd229human GRCh38 chr3: 133,968,521-133,973,217 , GRCh37.p13 chr3: 133,687,365-133,692,061 SLCO2A1
    nsv7044513inversion1nstd229human GRCh38 chr3: 131,210,998-138,882,695 , GRCh37.p13 chr3: 130,929,842-138,601,537 HSPA8P9, RNU6-1174P, 114 more genes
    nsv7041788inversion1nstd229human GRCh38 chr3: 133,903,647-134,206,077 , GRCh37.p13 chr3: 133,622,491-133,924,921 C3orf36, LINC02000, 4 more genes
    nsv7040617inversion1nstd229human GRCh38 chr3: 133,969,428-133,971,111 , GRCh37.p13 chr3: 133,688,272-133,689,955 SLCO2A1
    nsv7039302inversion1nstd229human GRCh38 chr3: 133,378,933-139,551,784 , GRCh37.p13 chr3: 133,097,777-139,270,626 ESYT3, DONSONP1, 99 more genes
    nsv6732120copy number variation1nstd229human GRCh38 chr3: 133,976,609-133,976,657 , GRCh37.p13 chr3: 133,695,453-133,695,501 SLCO2A1
    nsv6732072copy number variation1nstd229human GRCh38 chr3: 133,962,301-133,966,300 , GRCh37.p13 chr3: 133,681,145-133,685,144 SLCO2A1
    nsv6728533copy number variation1nstd229human GRCh38 chr3: 133,948,302-134,058,945 , GRCh37.p13 chr3: 133,667,146-133,777,789 SLCO2A1, LINC02000
    nsv6728444copy number variation1nstd229human GRCh38 chr3: 133,970,890-133,988,605 , GRCh37.p13 chr3: 133,689,734-133,707,449 SLCO2A1
    nsv6727444copy number variation1nstd229human GRCh38 chr3: 134,000,889-134,056,697 , GRCh37.p13 chr3: 133,719,733-133,775,541 LINC02000, SLCO2A1
    nsv6725668copy number variation1nstd229human GRCh38 chr3: 133,979,401-133,981,200 , GRCh37.p13 chr3: 133,698,245-133,700,044 SLCO2A1
    nsv6724830copy number variation1nstd229human GRCh38 chr3: 133,865,649-133,944,841 , GRCh37.p13 chr3: 133,584,493-133,663,685 RAB6B, SLCO2A1, 1 more genes
    nsv6722777copy number variation1nstd229human GRCh38 chr3: 133,888,101-133,945,500 , GRCh37.p13 chr3: 133,606,945-133,664,344 C3orf36, RAB6B, 1 more genes
    nsv6720485copy number variation1nstd229human GRCh38 chr3: 133,924,401-134,005,800 , GRCh37.p13 chr3: 133,643,245-133,724,644 SLCO2A1, C3orf36
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