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Items: 1 to 20 of 278

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148130copy number variation1nstd102humanPathogenic GRCh37 chr8: 36,763,176-50,929,707 , GRCh38.p12 chr8: 36,905,658-50,017,147 SNTG1, RN7SL806P, 193 more genes
    nsv7097797copy number variation1nstd102humanUncertain significance GRCh37 chr8: 43,002,091-43,159,912 , GRCh38.p12 chr8: 43,146,948-43,304,769 RNY5P6, VN1R45P, 6 more genes
    nsv6633054copy number variation1nstd224human GRCh37 chr8: 42,958,833-43,791,691 , GRCh38.p12 chr8: 43,103,690-43,936,548 POMK, POTEA, 11 more genes
    nsv6633053copy number variation3nstd224human GRCh37 chr8: 42,937,273-43,791,691 , GRCh38.p12 chr8: 43,082,130-43,936,548 POMK, SNX18P27, 12 more genes
    nsv6632990copy number variation2nstd224human GRCh37 chr8: 42,939,989-43,791,691 , GRCh38.p12 chr8: 43,084,846-43,936,548 FNTA, POTEA, 12 more genes
    nsv6632633copy number variation1nstd224human GRCh37 chr8: 43,145,487-43,791,691 , GRCh38.p12 chr8: 43,290,344-43,936,548 POTEA, LOC100420534, 4 more genes
    nsv6632631copy number variation1nstd224human GRCh37 chr8: 43,008,638-43,791,691 , GRCh38.p12 chr8: 43,153,495-43,936,548 VN1R46P, RNY5P6, 10 more genes
    nsv6632563copy number variation4nstd224human GRCh37 chr8: 43,052,839-43,791,691 , GRCh38.p12 chr8: 43,197,696-43,936,548 VN1R46P, LOC100420534, 9 more genes
    nsv6313701copy number variation1nstd102humanUncertain significance GRCh37 chr8: 42,162,574-48,757,095 , GRCh38.p12 chr8: 42,305,056-47,844,534 RNU1-124P, LOC728587, 66 more genes
    nsv6137291copy number variation1nstd213human GRCh37 chr8: 42,970,000-43,220,001 , GRCh38.p12 chr8: 43,114,857-43,364,858 POMK, HGSNAT, 7 more genes
    nsv6136050copy number variation1nstd213human GRCh37 chr8: 42,670,000-43,650,001 , GRCh38.p12 chr8: 42,814,857-43,794,858 FNTA, THAP1, 18 more genes
    nsv6136049copy number variation1nstd213human GRCh37 chr8: 42,190,000-43,790,001 , GRCh38.p12 chr8: 42,332,482-43,934,858 IKBKB, SLC20A2, 29 more genes
    nsv5973938inversion1nstd209human GRCh38 chr8: 41,482,982-43,307,552 , GRCh37.p13 chr8: 41,340,501-43,162,695 , ANK1, 46 more genes
    nsv5922141copy number variation1nstd209human GRCh38 chr8: 43,216,062-43,444,420 , GRCh37.p13 chr8: 43,071,205-43,299,563 , POTEA, 6 more genes
    nsv5917461copy number variation1nstd209human GRCh38 chr8: 41,299,580-47,196,853 , GRCh37.p13 chr8: 41,157,099-48,108,476 , AFG3L2P1, 81 more genes
    nsv5314350copy number variation1nstd204human GRCh38.p13 chr8: 43,267,670-43,319,396 , GRCh37.p13 chr8: 43,122,813-43,174,539 , POTEA, 2 more genes
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv4954401copy number variation1nstd200human GRCh38 chr8: 43,284,055-43,377,450 , GRCh37.p13 chr8: 43,139,198-43,232,593 , RNU6-104P, 1 more genes
    nsv4954400copy number variation1nstd200human GRCh38 chr8: 43,267,691-43,319,374 , GRCh37.p13 chr8: 43,122,834-43,174,517 , POTEA, 2 more genes
    nsv4954399copy number variation1nstd200human GRCh38 chr8: 43,230,931-43,772,662 , GRCh37.p13 chr8: 43,086,074-43,627,805 , RNU6-104P, 7 more genes
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