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Items: 1 to 20 of 165

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5894880copy number variation1nstd209human GRCh38 chr3: 149,380,188-149,380,351 , GRCh37.p13 chr3: 149,097,975-149,098,138 TM4SF1-AS1
    nsv5618068insertion1nstd207human GRCh38 chr3: 149,380,622-149,380,622 , GRCh37.p13 chr3: 149,098,409-149,098,409 TM4SF1-AS1
    nsv5617308insertion1nstd207human GRCh38 chr3: 149,380,809-149,380,809 , GRCh37.p13 chr3: 149,098,596-149,098,596 TM4SF1-AS1
    nsv5612715insertion1nstd207human GRCh38 chr3: 149,380,670-149,380,670 , GRCh37.p13 chr3: 149,098,457-149,098,457 TM4SF1-AS1
    nsv5612427insertion1nstd207human GRCh38 chr3: 149,380,218-149,380,218 , GRCh37.p13 chr3: 149,098,005-149,098,005 TM4SF1-AS1
    nsv5607278insertion2nstd207human GRCh38 chr3: 149,380,314-149,380,314 , GRCh37.p13 chr3: 149,098,101-149,098,101 TM4SF1-AS1
    nsv5606174insertion1nstd207human GRCh38 chr3: 149,380,250-149,380,250 , GRCh37.p13 chr3: 149,098,037-149,098,037 TM4SF1-AS1
    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
    nsv4914883copy number variation1nstd200human GRCh38 chr3: 149,379,050-149,391,768 , GRCh37.p13 chr3: 149,096,837-149,109,555 TM4SF1-AS1, LOC105374151
    nsv4765919insertion1nstd199human GRCh37 chr3: 149,097,918-149,097,918 , GRCh38.p12 chr3: 149,380,131-149,380,131 TM4SF1-AS1
    nsv4714455copy number variation1nstd195human GRCh37 chr3: 148,844,801-149,097,551 , GRCh38.p12 chr3: 149,127,014-149,379,764 , CP, 7 more genes
    nsv4708576copy number variation1nstd195human GRCh37 chr3: 149,099,001-149,162,101 , GRCh38.p12 chr3: 149,381,214-149,444,314 RPL32P8, TM4SF1-AS1, 1 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
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