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Items: 1 to 20 of 183

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096931copy number variation2nstd102humanUncertain significance GRCh37 chr3: 126,707,437-130,720,194 , GRCh38.p12 chr3: 126,988,594-131,001,350 JMJD4P1, MARK2P19, 104 more genes
    nsv7057230inversion1nstd229human GRCh38 chr3: 130,692,452-130,692,524 , GRCh37.p13 chr3: 130,411,296-130,411,368 PIK3R4
    nsv6736310copy number variation1nstd229human GRCh38 chr3: 130,719,801-130,833,400 , GRCh37.p13 chr3: 130,438,645-130,552,244 PIK3R4, GSTO3P, 3 more genes
    nsv6732682copy number variation1nstd229human GRCh38 chr3: 130,712,201-130,723,200 , GRCh37.p13 chr3: 130,431,045-130,442,044 PIK3R4
    nsv6724476copy number variation1nstd229human GRCh38 chr3: 130,411,878-130,916,442 , GRCh37.p13 chr3: 130,130,722-130,635,286 LOC105374108, CSRP2P2, 8 more genes
    nsv6722706copy number variation1nstd229human GRCh38 chr3: 130,619,701-130,986,505 , GRCh37.p13 chr3: 130,338,545-130,705,349 COL6A6, ATP2C1, 8 more genes
    nsv6720873copy number variation1nstd229human GRCh38 chr3: 130,699,106-130,702,259 , GRCh37.p13 chr3: 130,417,950-130,421,103 PIK3R4
    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
    nsv6571459inversion1nstd223human GRCh38 chr3: 130,720,349-130,720,890 , GRCh37.p13 chr3: 130,439,193-130,439,734 PIK3R4
    nsv6571351inversion1nstd223human GRCh38 chr3: 130,745,783-130,747,412 , GRCh37.p13 chr3: 130,464,627-130,466,256 LOC107986023, PIK3R4
    nsv6373828copy number variation1nstd223human GRCh38 chr3: 130,695,907-130,696,419 , GRCh37.p13 chr3: 130,414,751-130,415,263 PIK3R4
    nsv6369274copy number variation1nstd223human GRCh38 chr3: 130,682,916-130,683,376 , GRCh37.p13 chr3: 130,401,760-130,402,220 PIK3R4
    nsv6364611copy number variation1nstd223human GRCh38 chr3: 130,695,191-130,695,932 , GRCh37.p13 chr3: 130,414,035-130,414,776 PIK3R4
    nsv6363577copy number variation1nstd223human GRCh38 chr3: 130,724,401-130,725,700 , GRCh37.p13 chr3: 130,443,245-130,444,544 PIK3R4
    nsv6363133copy number variation1nstd223human GRCh38 chr3: 130,729,601-130,730,700 , GRCh37.p13 chr3: 130,448,445-130,449,544 PIK3R4
    nsv6361058copy number variation1nstd223human GRCh38 chr3: 130,735,212-130,735,681 , GRCh37.p13 chr3: 130,454,056-130,454,525 PIK3R4
    nsv6360060copy number variation1nstd223human GRCh38 chr3: 130,619,701-130,986,505 , GRCh37.p13 chr3: 130,338,545-130,705,349 LOC107986023, RN7SKP212, 8 more genes
    nsv6359708copy number variation1nstd223human GRCh38 chr3: 130,710,101-130,711,200 , GRCh37.p13 chr3: 130,428,945-130,430,044 PIK3R4
    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
    nsv6292980mobile element insertion1nstd186human GRCh37 chr3: 130,453,357-130,453,408 , GRCh38.p12 chr3: 130,734,513-130,734,564 PIK3R4
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