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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5889578copy number variation1nstd209human GRCh38 chr6: 35,501,540-35,501,623 , GRCh37.p13 chr6: 35,469,317-35,469,400 TULP1
    nsv5674010copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 35,476,986-35,480,467 , GRCh38.p12 chr6: 35,509,209-35,512,690 TULP1
    nsv5566435copy number variation1nstd207human GRCh38 chr6: 35,501,540-35,501,623 , GRCh37.p13 chr6: 35,469,317-35,469,400 TULP1
    nsv5471897copy number variation1nstd206human GRCh38 chr6: 35,501,538-35,501,624 , GRCh37.p13 chr6: 35,469,315-35,469,401 TULP1
    nsv5471503copy number variation1nstd206human GRCh38 chr6: 35,507,917-35,545,974 , GRCh37.p13 chr6: 35,475,694-35,513,751 TULP1, LOC101929309
    nsv5463515copy number variation1nstd206human GRCh38 chr6: 35,507,124-35,507,205 , GRCh37.p13 chr6: 35,474,901-35,474,982 TULP1
    nsv5387348copy number variation1nstd186human GRCh37 chr6: 35,469,314-35,469,401 , GRCh38.p12 chr6: 35,501,537-35,501,624 TULP1
    nsv5381531copy number variation1nstd102humanUncertain significance GRCh37 chr6: 35,476,986-35,565,181 , GRCh38.p12 chr6: 35,509,209-35,597,404 TULP1, RPS15AP19, 2 more genes
    nsv5378397translocation1nstd200human GRCh38 chr6: 35,511,791-35,511,791 , GRCh38 chr6: 35,506,205-35,506,205 , GRCh37.p13 chr6: 35,473,982-35,473,982 , GRCh37.p13 chr6: 35,479,568-35,479,568 TULP1
    nsv5378396translocation1nstd200human GRCh38 chr6: 35,512,318-35,512,318 , GRCh38 chr6: 35,501,421-35,501,421 , GRCh37.p13 chr6: 35,480,095-35,480,095 , GRCh37.p13 chr6: 35,469,198-35,469,198 TULP1
    nsv5362845translocation1nstd200human GRCh38 chr6: 35,512,313-35,512,313 , GRCh38 chr6: 35,506,200-35,506,200 , GRCh37.p13 chr6: 35,473,977-35,473,977 , GRCh37.p13 chr6: 35,480,090-35,480,090 TULP1
    nsv5341423translocation1nstd200human GRCh37 chr6: 35,469,198-35,469,198 , GRCh37 chr6: 35,480,095-35,480,095 , GRCh38.p12 chr6: 35,501,421-35,501,421 , GRCh38.p12 chr6: 35,512,318-35,512,318 TULP1
    nsv5339802translocation1nstd200human GRCh37 chr6: 35,473,982-35,473,982 , GRCh37 chr6: 35,479,568-35,479,568 , GRCh38.p12 chr6: 35,511,791-35,511,791 , GRCh38.p12 chr6: 35,506,205-35,506,205 TULP1
    nsv5337243translocation1nstd200human GRCh37 chr6: 35,473,977-35,473,977 , GRCh37 chr6: 35,480,090-35,480,090 , GRCh38.p12 chr6: 35,512,313-35,512,313 , GRCh38.p12 chr6: 35,506,200-35,506,200 TULP1
    nsv5200371copy number variation1nstd102humanPathogenic GRCh37 chr6: 34,401,304-38,435,497 , GRCh38.p12 chr6: 34,433,527-38,467,721 RPS15AP19, FKBP5, 95 more genes
    nsv5031134inversion1nstd200human GRCh38 chr6: 35,178,266-40,407,996 , GRCh37.p13 chr6: 35,146,043-40,375,735 , LOC105375040, 114 more genes
    nsv4934619copy number variation1nstd200human GRCh38 chr6: 35,510,332-35,534,220 , GRCh37.p13 chr6: 35,478,109-35,501,997 TULP1
    nsv4934618copy number variation1nstd200human GRCh38 chr6: 35,507,870-35,546,036 , GRCh37.p13 chr6: 35,475,647-35,513,813 TULP1, LOC101929309
    nsv4872414inversion1nstd200human GRCh37 chr6: 35,146,053-40,375,735 , GRCh38.p12 chr6: 35,178,276-40,407,996 , RPL36P9, 114 more genes
    nsv4828635copy number variation1nstd200human GRCh37 chr6: 35,478,109-35,501,997 , GRCh38.p12 chr6: 35,510,332-35,534,220 TULP1
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