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Items: 1 to 20 of 186

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145372insertion1nstd232human GRCh37.p13 chr3: 185,644,522-185,644,522 , GRCh38.p12 chr3: 185,926,734-185,926,734 TRA2B
    nsv7139320insertion1nstd232human GRCh37.p13 chr3: 185,643,416-185,643,416 , GRCh38.p12 chr3: 185,925,628-185,925,628 TRA2B
    nsv7040429inversion1nstd229human GRCh38 chr3: 184,379,670-192,292,047 , GRCh37.p13 chr3: 184,097,458-192,009,836 LOC107986163, RPL34P10, 123 more genes
    nsv6738070copy number variation1nstd229human GRCh38 chr3: 185,938,318-185,943,061 , GRCh37.p13 chr3: 185,656,106-185,660,849 TRA2B
    nsv6734884copy number variation1nstd229human GRCh38 chr3: 185,857,401-185,915,800 , GRCh37.p13 chr3: 185,575,189-185,633,588 TRA2B
    nsv6732245copy number variation1nstd229human GRCh38 chr3: 185,936,701-186,088,900 , GRCh37.p13 chr3: 185,654,489-185,806,689 ETV5, NMRAL2P, 1 more genes
    nsv6729014copy number variation1nstd229human GRCh38 chr3: 185,932,015-186,010,204 , GRCh37.p13 chr3: 185,649,803-185,727,993 NMRAL2P, TRA2B
    nsv6727659copy number variation1nstd229human GRCh38 chr3: 185,935,901-185,973,300 , GRCh37.p13 chr3: 185,653,689-185,691,089 NMRAL2P, TRA2B
    nsv6722756copy number variation1nstd229human GRCh38 chr3: 185,918,101-186,105,400 , GRCh37.p13 chr3: 185,635,889-185,823,189 TRA2B, NMRAL2P, 1 more genes
    nsv6722228copy number variation1nstd229human GRCh38 chr3: 185,935,930-185,936,031 , GRCh37.p13 chr3: 185,653,718-185,653,819 TRA2B
    nsv6721680copy number variation1nstd229human GRCh38 chr3: 185,913,027-185,914,281 , GRCh37.p13 chr3: 185,630,815-185,632,069 TRA2B
    nsv6636645copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 184,170,962-188,047,867 , GRCh38.p12 chr3: 184,453,174-188,330,079 AHSG, BCL6, 80 more genes
    nsv6634371copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 171,549,421-198,022,430 , GRCh38.p12 chr3: 171,831,631-198,235,559 ACTL6A, AHSG, 466 more genes
    nsv6369675copy number variation1nstd223human GRCh38 chr3: 185,915,407-185,915,993 , GRCh37.p13 chr3: 185,633,195-185,633,781 TRA2B
    nsv6366480copy number variation1nstd223human GRCh38 chr3: 185,912,987-185,914,306 , GRCh37.p13 chr3: 185,630,775-185,632,094 TRA2B
    nsv6364241copy number variation1nstd223human GRCh38 chr3: 185,858,849-185,948,316 , GRCh37.p13 chr3: 185,576,637-185,666,104 TRA2B
    nsv6362267copy number variation1nstd223human GRCh38 chr3: 185,916,701-185,918,500 , GRCh37.p13 chr3: 185,634,489-185,636,288 TRA2B
    nsv6360104copy number variation1nstd223human GRCh38 chr3: 185,910,832-185,991,463 , GRCh37.p13 chr3: 185,628,620-185,709,252 NMRAL2P, TRA2B
    nsv6315437copy number variation1nstd102humanPathogenic GRCh37 chr3: 183,498,520-197,851,986 , GRCh38.p12 chr3: 183,780,732-198,125,115 LOC105374291, GP5, 315 more genes
    nsv6315366copy number variation1nstd102humanPathogenic GRCh37 chr3: 183,556,940-188,083,060 , GRCh38.p12 chr3: 183,839,152-188,365,272 MASP1, PSMD10P2, 115 more genes
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