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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5896507copy number variation1nstd209human GRCh38 chr3: 149,210,172-149,227,712 , GRCh37.p13 chr3: 148,927,959-148,945,499 LOC101927942, CP
    nsv5555704sequence alteration1nstd206human GRCh38 chr3: 149,217,851-149,222,772 , GRCh37.p13 chr3: 148,935,638-148,940,559 CP, LOC101927942
    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
    nsv4912314copy number variation1nstd200human GRCh38 chr3: 149,221,380-149,223,989 , GRCh37.p13 chr3: 148,939,167-148,941,776 CP, LOC101927942
    nsv4714455copy number variation1nstd195human GRCh37 chr3: 148,844,801-149,097,551 , GRCh38.p12 chr3: 149,127,014-149,379,764 , CP, 7 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
    nsv4674717copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 144,053,029-150,272,658 , GRCh38.p12 chr3: 144,334,187-150,554,871 AGTR1, CP, 83 more genes
    nsv4584980copy number variation1nstd183human GRCh37 chr3: 148,854,793-149,130,499 , GRCh38.p12 chr3: 149,137,006-149,412,712 , CPHL1P, 8 more genes
    nsv4452962copy number variation1nstd102humanUncertain significance GRCh37 chr3: 148,855,964-149,227,161 , GRCh38.p12 chr3: 149,138,177-149,509,374 RPL32P8, TM4SF1, 11 more genes
    nsv4451199copy number variation1nstd102humanUncertain significance GRCh37 chr3: 148,855,964-149,130,487 , GRCh38.p12 chr3: 149,138,177-149,412,700 CP, TM4SF1, 7 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
    nsv4102084copy number variation1nstd166human GRCh37.p13 chr3: 148,939,167-148,941,776 , GRCh38.p12 chr3: 149,221,380-149,223,989 CP, LOC101927942
    nsv3970457copy number variation1nstd168human GRCh38 chr3: 149,215,312-149,253,291 , GRCh37.p13 chr3: 148,933,099-148,971,078 CP, LOC101927942, 1 more genes
    nsv3924004copy number variation1nstd102humanUncertain significance NCBI36 chr3: 150,337,830-150,620,377 , GRCh37 chr3: 148,855,140-149,137,687 , GRCh38 chr3: 149,137,353-149,419,900 TM4SF1-AS1, HPS3, 7 more genes
    nsv3920790copy number variation1nstd102humanPathogenic GRCh38 chr3: 134,257,180-149,729,538 , NCBI36 chr3: 135,458,712-150,930,015 , GRCh37 chr3: 133,976,022-149,447,325 TFDP2, RPL7L1P7, 203 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
    nsv3918784copy number variation1nstd102humanPathogenic GRCh37 chr3: 147,160,353-178,240,319 , GRCh38 chr3: 147,442,566-178,522,531 , NCBI36 chr3: 148,643,043-179,723,013 LOC105374167, LOC105374187, 394 more genes
    nsv3918692copy number variation1nstd102humanPathogenic GRCh38 chr3: 147,521,892-198,096,565 , GRCh37 chr3: 147,239,679-197,823,436 , NCBI36 chr3: 148,722,369-199,307,833 LOC105374179, LINC02038, 785 more genes
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