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Items: 1 to 20 of 808

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7055656inversion1nstd229human GRCh38 chr2: 169,869,325-169,877,663 , GRCh37.p13 chr2: 170,725,835-170,734,173 UBR3
    nsv7053026inversion1nstd229human GRCh38 chr2: 170,012,731-170,012,761 , GRCh37.p13 chr2: 170,869,241-170,869,271 UBR3
    nsv7043962inversion1nstd229human GRCh38 chr2: 169,872,641-169,877,136 , GRCh37.p13 chr2: 170,729,151-170,733,646 UBR3
    nsv7043764inversion1nstd229human GRCh38 chr2: 169,756,513-170,924,608 , GRCh37.p13 chr2: 170,613,023-171,781,118 LINC01124, METTL5, 17 more genes
    nsv7039897inversion1nstd229human GRCh38 chr2: 169,884,886-169,884,942 , GRCh37.p13 chr2: 170,741,396-170,741,452 UBR3
    nsv7039492inversion1nstd229human GRCh38 chr2: 169,907,682-169,907,772 , GRCh37.p13 chr2: 170,764,192-170,764,282 UBR3
    nsv6697982copy number variation1nstd229human GRCh38 chr2: 169,890,550-169,891,076 , GRCh37.p13 chr2: 170,747,060-170,747,586 UBR3
    nsv6697372copy number variation1nstd229human GRCh38 chr2: 169,988,465-170,447,481 , GRCh37.p13 chr2: 170,844,975-171,303,991 NSA2P5, UBR3, 3 more genes
    nsv6696751copy number variation1nstd229human GRCh38 chr2: 169,980,931-169,980,949 , GRCh37.p13 chr2: 170,837,441-170,837,459 UBR3
    nsv6696550copy number variation1nstd229human GRCh38 chr2: 169,730,701-169,861,097 , GRCh37.p13 chr2: 170,587,211-170,717,607 METTL5, PHOSPHO2-KLHL23, 7 more genes
    nsv6695773copy number variation1nstd229human GRCh38 chr2: 169,849,647-169,850,563 , GRCh37.p13 chr2: 170,706,157-170,707,073 UBR3
    nsv6695547copy number variation1nstd229human GRCh38 chr2: 169,843,920-169,850,184 , GRCh37.p13 chr2: 170,700,430-170,706,694 UBR3
    nsv6695172copy number variation1nstd229human GRCh38 chr2: 169,863,928-170,054,070 , GRCh37.p13 chr2: 170,720,438-170,910,580 UBR3
    nsv6694941copy number variation1nstd229human GRCh38 chr2: 169,845,181-169,854,392 , GRCh37.p13 chr2: 170,701,691-170,710,902 UBR3
    nsv6692822copy number variation1nstd229human GRCh38 chr2: 169,873,499-169,873,615 , GRCh37.p13 chr2: 170,730,009-170,730,125 UBR3
    nsv6692755copy number variation1nstd229human GRCh38 chr2: 169,960,344-169,961,366 , GRCh37.p13 chr2: 170,816,854-170,817,876 UBR3
    nsv6692678copy number variation1nstd229human GRCh38 chr2: 170,055,952-170,056,022 , GRCh37.p13 chr2: 170,912,462-170,912,532 UBR3
    nsv6691752copy number variation1nstd229human GRCh38 chr2: 169,836,323-169,843,511 , GRCh37.p13 chr2: 170,692,833-170,700,021 UBR3
    nsv6691070copy number variation1nstd229human GRCh38 chr2: 170,057,240-170,059,958 , GRCh37.p13 chr2: 170,913,750-170,916,468 UBR3
    nsv6689606copy number variation1nstd229human GRCh38 chr2: 169,864,001-169,890,000 , GRCh37.p13 chr2: 170,720,511-170,746,510 UBR3
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