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Items: 1 to 20 of 145

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7047569inversion1nstd229human GRCh38 chr3: 152,490,812-161,531,961 , GRCh37.p13 chr3: 152,208,601-161,249,749 RPS2P19, LOC112268450, 128 more genes
    nsv6731234copy number variation1nstd229human GRCh38 chr3: 157,586,937-158,968,270 , GRCh37.p13 chr3: 157,304,726-158,686,059 LOC100287290, LILRA2P1, 17 more genes
    nsv6722096copy number variation1nstd229human GRCh38 chr3: 157,990,842-158,993,928 , GRCh37.p13 chr3: 157,708,631-158,711,717 RPL35AP9, GFM1, 15 more genes
    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
    nsv6366053copy number variation1nstd223human GRCh38 chr3: 158,094,001-158,119,800 , GRCh37.p13 chr3: 157,811,790-157,837,589 SHOX2, RSRC1
    nsv6358489copy number variation1nstd223human GRCh38 chr3: 158,052,627-158,113,670 , GRCh37.p13 chr3: 157,770,416-157,831,459 SHOX2, RSRC1
    nsv6313678copy number variation1nstd102humanPathogenic GRCh37 chr3: 145,486,960-160,504,834 , GRCh38.p12 chr3: 145,769,173-160,787,046 RNU6-901P, RPL32P8, 229 more genes
    nsv6313664copy number variation1nstd102humanUncertain significance GRCh37 chr3: 156,768,935-160,158,553 , GRCh38.p12 chr3: 157,051,146-160,440,765 LOC105374179, RPL15P6, 49 more genes
    nsv6290273copy number variation1nstd102humanPathogenic GRCh37 chr3: 142,729,607-157,921,084 , GRCh38.p12 chr3: 143,010,765-158,203,295 LINC02066, TM4SF1-AS1, 206 more genes
    nsv6290244copy number variation1nstd102humanPathogenic GRCh37 chr3: 143,439,359-165,252,122 , GRCh38.p12 chr3: 143,720,517-165,534,334 LOC102724145, C3orf80, 273 more genes
    nsv6134788copy number variation1nstd213human GRCh37 chr3: 155,010,000-169,630,001 , GRCh38.p12 chr3: 155,292,211-169,912,213 , BCHE, 171 more genes
    nsv5991699copy number variation1nstd212human GRCh38 chr3: 158,106,571-158,106,629 , GRCh37.p13 chr3: 157,824,360-157,824,418 SHOX2
    nsv5722728mobile element insertion1nstd211human GRCh38 chr3: 158,099,282-158,099,282 , GRCh37.p13 chr3: 157,817,071-157,817,071 SHOX2
    nsv5559668mobile element insertion1nstd206human GRCh38 chr3: 158,099,282-158,099,282 , GRCh37.p13 chr3: 157,817,071-157,817,071 SHOX2
    nsv5381765copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911 MBNL1-AS1, LOC107986138, 339 more genes
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4744889copy number variation1nstd199human GRCh37 chr3: 157,824,352-157,824,409 , GRCh38.p12 chr3: 158,106,563-158,106,620 SHOX2
    nsv4728531copy number variation1nstd102humanUncertain significance GRCh37 chr3: 157,666,169-158,146,714 , GRCh38.p12 chr3: 157,948,380-158,428,925 LILRA2P1, RSRC1, 2 more genes
    nsv4684209copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,145,289-162,275,610 , GRCh38.p12 chr3: 138,426,447-162,557,822 MTAPP1, PLS1, 339 more genes
    nsv4684148copy number variation1nstd102humanUncertain significance GRCh37 chr3: 156,812,581-160,154,747 , GRCh38.p12 chr3: 157,094,792-160,436,959 RSRC1, SMC4, 48 more genes
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