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Items: 1 to 20 of 684

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076524inversion1nstd229human GRCh38 chr9: 37,997,199-38,003,162 , GRCh37.p13 chr9: 37,997,196-38,003,159 SHB
    nsv7066167inversion1nstd229human GRCh38 chr9: 38,065,022-38,080,468 , GRCh37.p13 chr9: 38,065,019-38,080,465 LOC105376039, SHB
    nsv7061632inversion1nstd229human GRCh38 chr9: 37,968,670-37,968,714 , GRCh37.p13 chr9: 37,968,667-37,968,711 SHB
    nsv7060812inversion1nstd229human GRCh38 chr9: 38,067,025-38,077,964 , GRCh37.p13 chr9: 38,067,022-38,077,961 LOC105376039, SHB
    nsv7060440inversion1nstd229human GRCh38 chr9: 33,533,890-38,610,880 , GRCh37.p13 chr9: 33,533,888-38,610,877 FRMPD1, PTENP1, 182 more genes
    nsv7058978inversion1nstd229human GRCh38 chr9: 33,570,636-38,550,207 , GRCh37.p13 chr9: 33,570,634-38,550,204 TRBV29OR9-2, SPMIP6, 180 more genes
    nsv7058366inversion1nstd229human GRCh38 chr9: 38,028,385-38,028,510 , GRCh37.p13 chr9: 38,028,382-38,028,507 SHB
    nsv6877583copy number variation1nstd229human GRCh38 chr9: 37,969,418-37,972,383 , GRCh37.p13 chr9: 37,969,415-37,972,380 SHB
    nsv6877487copy number variation1nstd229human GRCh38 chr9: 37,920,300-37,920,336 , GRCh37.p13 chr9: 37,920,297-37,920,333 SHB
    nsv6876943copy number variation1nstd229human GRCh38 chr9: 37,932,652-37,934,338 , GRCh37.p13 chr9: 37,932,649-37,934,335 SHB
    nsv6874268copy number variation1nstd229human GRCh38 chr9: 38,017,316-38,017,573 , GRCh37.p13 chr9: 38,017,313-38,017,570 SHB
    nsv6872299copy number variation1nstd229human GRCh38 chr9: 38,000,110-38,004,204 , GRCh37.p13 chr9: 38,000,107-38,004,201 SHB
    nsv6869098copy number variation1nstd229human GRCh38 chr9: 37,958,411-37,958,626 , GRCh37.p13 chr9: 37,958,408-37,958,623 SHB
    nsv6868186copy number variation1nstd229human GRCh38 chr9: 37,998,267-38,009,223 , GRCh37.p13 chr9: 37,998,264-38,009,220 SHB
    nsv6867338copy number variation1nstd229human GRCh38 chr9: 38,059,801-38,084,600 , GRCh37.p13 chr9: 38,059,798-38,084,597 LOC105376039, SHB
    nsv6866696copy number variation1nstd229human GRCh38 chr9: 37,998,901-38,005,300 , GRCh37.p13 chr9: 37,998,898-38,005,297 SHB
    nsv6863071copy number variation1nstd229human GRCh38 chr9: 38,034,472-38,042,562 , GRCh37.p13 chr9: 38,034,469-38,042,559 SHB
    nsv6860814copy number variation1nstd229human GRCh38 chr9: 38,063,061-38,063,459 , GRCh37.p13 chr9: 38,063,058-38,063,456 SHB
    nsv6858948copy number variation1nstd229human GRCh38 chr9: 37,926,854-38,721,465 , GRCh37.p13 chr9: 37,926,851-38,721,462 CYP4F33P, ANKRD18A, 19 more genes
    nsv6858886copy number variation1nstd229human GRCh38 chr9: 38,020,337-38,026,402 , GRCh37.p13 chr9: 38,020,334-38,026,399 SHB
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