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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
    nsv6125946insertion1nstd186human GRCh37 chr6: 36,980,798-36,980,814 , GRCh38.p12 chr6: 37,013,022-37,013,038 FGD2
    nsv5955629insertion1nstd209human GRCh38 chr6: 37,012,988-37,012,988 , GRCh37.p13 chr6: 36,980,764-36,980,764 FGD2
    nsv5950024insertion1nstd209human GRCh38 chr6: 37,028,615-37,028,615 , GRCh37.p13 chr6: 36,996,391-36,996,391 FGD2
    nsv5902805copy number variation1nstd209human GRCh38 chr6: 37,026,537-37,026,592 , GRCh37.p13 chr6: 36,994,313-36,994,368 FGD2
    nsv5643594insertion1nstd207human GRCh38 chr6: 37,012,986-37,012,986 , GRCh37.p13 chr6: 36,980,762-36,980,762 FGD2
    nsv5534128insertion1nstd206human GRCh38 chr6: 37,013,022-37,013,038 , GRCh37.p13 chr6: 36,980,798-36,980,814 FGD2
    nsv5344450translocation1nstd200human GRCh37 chr6: 36,994,297-36,994,297 , GRCh37 chr6: 36,994,369-36,994,369 , GRCh38.p12 chr6: 37,026,593-37,026,593 , GRCh38.p12 chr6: 37,026,521-37,026,521 FGD2
    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
    nsv4940929copy number variation1nstd200human GRCh38 chr6: 37,009,173-37,009,832 , GRCh37.p13 chr6: 36,976,949-36,977,608 FGD2
    nsv4934637copy number variation1nstd200human GRCh38 chr6: 36,809,158-37,140,216 , GRCh37.p13 chr6: 36,776,934-37,107,992 C6orf89, MTCH1, 6 more genes
    nsv4872414inversion1nstd200human GRCh37 chr6: 35,146,053-40,375,735 , GRCh38.p12 chr6: 35,178,276-40,407,996 , RPL36P9, 114 more genes
    nsv4816045copy number variation1nstd200human GRCh37 chr6: 36,976,949-36,977,608 , GRCh38.p12 chr6: 37,009,173-37,009,832 FGD2
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756771insertion1nstd199human GRCh37 chr6: 36,980,765-36,980,765 , GRCh38.p12 chr6: 37,012,989-37,012,989 FGD2
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv4598570copy number variation1nstd183human GRCh37 chr6: 36,988,276-36,988,370 , GRCh38.p12 chr6: 37,020,500-37,020,594 FGD2
    nsv4598568copy number variation1nstd183human GRCh37 chr6: 36,940,805-37,050,771 , GRCh38.p12 chr6: 36,973,029-37,082,995 COX6A1P2, FGD2, 1 more genes
    nsv4455569copy number variation1nstd102humanUncertain significance GRCh37 chr6: 36,776,798-37,106,051 , GRCh38.p12 chr6: 36,809,022-37,138,275 PI16, MTCH1, 6 more genes
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