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Items: 1 to 20 of 132

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6555836inversion1nstd223human GRCh38 chr3: 152,336,791-152,342,231 , GRCh37.p13 chr3: 152,054,580-152,060,020 MBNL1, TMEM14EP
    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
    nsv6313632copy number variation1nstd102humanUncertain significance GRCh37 chr3: 151,147,204-154,845,718 , GRCh38.p12 chr3: 151,429,416-155,127,929 LOC105374171, ARHGEF26-AS1, 42 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
    nsv6134674copy number variation1nstd213human GRCh37 chr3: 150,600,000-153,170,001 , GRCh38.p12 chr3: 150,882,213-153,452,212 CLRN1-AS1, MBNL1-AS1, 37 more genes
    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
    nsv5235148copy number variation1nstd204human GRCh38.p13 chr3: 152,320,570-152,349,428 , GRCh37.p13 chr3: 152,038,359-152,067,217 MBNL1, TMEM14EP
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4912390copy number variation1nstd200human GRCh38 chr3: 151,409,405-152,510,511 , GRCh37.p13 chr3: 151,127,193-152,228,300 , IGSF10, 17 more genes
    nsv4728455copy number variation1nstd102humanUncertain significance GRCh37 chr3: 151,702,938-152,648,714 , GRCh38.p12 chr3: 151,985,149-152,930,925 ATP5MGP5, TMEM14EP, 6 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
    nsv4674301copy number variation1nstd102humanPathogenic GRCh37 chr3: 149,404,255-152,786,331 , GRCh38.p12 chr3: 149,686,468-153,068,542 EIF3JP2, IGSF10, 63 more genes
    nsv4587621copy number variation1nstd183human GRCh37 chr3: 151,897,062-152,174,158 , GRCh38.p12 chr3: 152,179,273-152,456,369 , MBNL1, 3 more genes
    nsv4387977copy number variation1nstd173human GRCh37 chr3: 151,924,042-152,070,136 , GRCh38.p12 chr3: 152,206,253-152,352,347 , TMEM14EP, 2 more genes
    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
    nsv3922071copy number variation1nstd102humanLikely pathogenic NCBI36 chr3: 152,629,894-156,319,129 , GRCh37 chr3: 151,147,204-154,836,435 , GRCh38 chr3: 151,429,416-155,118,646 AADAC, MBNL1, 42 more genes
    nsv3918981copy number variation1nstd102humanPathogenic GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446 LINC02614, LINC02054, 1469 more genes
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