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Items: 1 to 20 of 138

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5962473insertion1nstd209human GRCh38 chr3: 149,322,905-149,322,905 , GRCh37.p13 chr3: 149,040,692-149,040,692 TM4SF18
    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
    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
    nsv4468800mobile element insertion1nstd166human GRCh37.p13 chr3: 149,043,177-149,043,177 , GRCh38.p12 chr3: 149,325,390-149,325,390 TM4SF18
    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
    nsv4372427copy number variation1nstd173human GRCh37 chr3: 149,000,201-149,062,461 , GRCh38.p12 chr3: 149,282,414-149,344,674 , TM4SF18
    nsv4369894copy number variation1nstd173human GRCh37 chr3: 149,000,201-149,066,126 , GRCh38.p12 chr3: 149,282,414-149,348,339 , TM4SF18
    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
    nsv4103675copy number variation1nstd166human GRCh37.p13 chr3: 149,047,679-149,047,746 , GRCh38.p12 chr3: 149,329,892-149,329,959 TM4SF18
    nsv4103459copy number variation1nstd166human GRCh37.p13 chr3: 149,039,299-149,043,700 , GRCh38.p12 chr3: 149,321,512-149,325,913 TM4SF18
    nsv4097367copy number variation1nstd166human GRCh37.p13 chr3: 149,049,984-149,050,654 , GRCh38.p12 chr3: 149,332,197-149,332,867 TM4SF18
    nsv3961722copy number variation1nstd168human GRCh38 chr3: 149,328,358-149,397,129 , GRCh37.p13 chr3: 149,046,145-149,114,916 LOC105374151, TM4SF18, 3 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
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