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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5434854copy number variation1nstd206human GRCh38 chr3: 132,656,534-132,656,590 , GRCh37.p13 chr3: 132,375,378-132,375,434 UBA5, NPHP3-ACAD11, 1 more genes
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4920193copy number variation1nstd200human GRCh38 chr3: 132,679,116-132,679,880 , GRCh37.p13 chr3: 132,397,960-132,398,724 NPHP3, NPHP3-ACAD11, 1 more genes
    nsv4920192copy number variation1nstd200human GRCh38 chr3: 132,654,430-132,657,087 , GRCh37.p13 chr3: 132,373,274-132,375,931 NPHP3-ACAD11, UBA5, 1 more genes
    nsv4920191copy number variation1nstd200human GRCh38 chr3: 132,653,604-132,653,665 , GRCh37.p13 chr3: 132,372,448-132,372,509 NPHP3-ACAD11, ACAD11, 1 more genes
    nsv4920187copy number variation1nstd200human GRCh38 chr3: 132,603,776-132,991,813 , GRCh37.p13 chr3: 132,322,620-132,710,657 NPHP3, UBA5, 5 more genes
    nsv4914773copy number variation1nstd200human GRCh38 chr3: 132,365,682-133,204,470 , GRCh37.p13 chr3: 132,084,526-132,923,314 NPHP3, ACKR4, 11 more genes
    nsv4728534copy number variation1nstd102humanUncertain significance GRCh37 chr3: 132,355,550-132,988,372 , GRCh38.p12 chr3: 132,636,706-133,269,528 NPHP3, ACAD11, 7 more genes
    nsv4682513copy number variation1nstd102humanPathogenic GRCh37 chr3: 132,345,535-132,441,199 , GRCh38.p12 chr3: 132,626,691-132,722,355 NPHP3, UBA5, 4 more genes
    nsv4682381copy number variation1nstd102humanUncertain significance GRCh37 chr3: 132,184,839-132,441,199 , GRCh38.p12 chr3: 132,465,995-132,722,355 HSPA8P19, UBA5, 6 more genes
    nsv4596055copy number variation1nstd183human GRCh37 chr3: 131,866,636-132,504,231 , GRCh38.p12 chr3: 132,147,792-132,785,387 ACKR4, NPHP3-AS1, 15 more genes
    nsv4587244copy number variation1nstd183human GRCh37 chr3: 132,174,467-132,965,626 , GRCh38.p12 chr3: 132,455,623-133,246,782 TMEM108, NPHP3-AS1, 9 more genes
    nsv4569392mobile element insertion1nstd166human GRCh37.p13 chr3: 132,386,560-132,386,560 , GRCh38.p12 chr3: 132,667,716-132,667,716 NPHP3-ACAD11, UBA5
    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
    nsv4104750copy number variation1nstd166human GRCh37.p13 chr3: 132,397,960-132,398,724 , GRCh38.p12 chr3: 132,679,116-132,679,880 NPHP3, UBA5, 1 more genes
    nsv4101507copy number variation1nstd166human GRCh37.p13 chr3: 132,322,620-132,710,657 , GRCh38.p12 chr3: 132,603,776-132,991,813 NPHP3, UBA5, 5 more genes
    nsv3923363copy number variation1nstd102humanUncertain significance NCBI36 chr3: 133,841,054-134,174,160 , GRCh37 chr3: 132,358,364-132,691,470 , GRCh38 chr3: 132,639,520-132,972,626 NPHP3, HSPA8P19, 5 more genes
    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
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