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Items: 1 to 20 of 936

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148253copy number variation1nstd102humanPathogenic GRCh38 chr8: 449,893-23,854,904 , GRCh37.p13 chr8: 399,893-23,712,417 ENTPD4, LOC100421446, 447 more genes
    nsv7148131copy number variation1nstd102humanPathogenic GRCh37 chr8: 10,501-11,142,629 , GRCh38.p12 chr8: 60,501-11,285,120 XKR6, FAM90A11, 224 more genes
    nsv7148128copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 10,501-6,614,959 , GRCh38.p12 chr8: 60,501-6,757,438 ANGPT2, CLN8, 67 more genes
    nsv7145769copy number variation1nstd232human GRCh37.p13 chr8: 2,078,116-2,078,165 , GRCh38.p12 chr8: 2,130,128-2,130,177 , GRCh38.p12 chr8|NT_187576.1: 313,326-313,375 MYOM2
    nsv7144554copy number variation1nstd232human GRCh37.p13 chr8: 2,029,089-2,029,140 , GRCh38.p12 chr8|NT_187576.1: 264,299-264,350 MYOM2
    nsv7143852copy number variation1nstd232human GRCh37.p13 chr8: 2,033,733-2,033,806 , GRCh38.p12 chr8: 2,085,599-2,085,672 , GRCh38.p12 chr8|NT_187576.1: 268,943-269,016 MYOM2
    nsv7140715insertion1nstd232human GRCh37.p13 chr8: 2,034,184-2,034,184 , GRCh38.p12 chr8: 2,086,407-2,086,407 , GRCh38.p12 chr8|NT_187576.1: 269,394-269,394 MYOM2
    nsv7139976copy number variation1nstd232human GRCh37.p13 chr8: 2,078,313-2,078,404 , GRCh38.p12 chr8: 2,130,325-2,130,416 , GRCh38.p12 chr8|NT_187576.1: 313,523-313,614 MYOM2
    nsv7074214inversion1nstd229human GRCh38 chr8: 1,202,764-2,370,937 , GRCh37.p13 chr8: 1,152,764-1,965,389 LOC105377781, MYOM2, 21 more genes
    nsv7074012inversion1nstd229human GRCh37.p13 chr8|NW_003571042.1: 3,934-590,421 , GRCh38 chr8: 2,021,162-2,883,254 LOC105377782, LOC105377785, 7 more genes
    nsv7073316inversion1nstd229human GRCh38 chr8: 2,080,115-2,488,538 , GRCh37.p13 chr8|NW_003571042.1: 62,807-324,019 LOC105377781, LOC105377784, 3 more genes
    nsv7072618inversion1nstd229human GRCh37.p13 chr8|NW_003571042.1: 65,632-324,019 , GRCh38 chr8: 2,082,889-2,561,321 LINC03021, LOC105377783, 4 more genes
    nsv7068644inversion1nstd229human GRCh38 chr8: 496,129-6,118,991 , GRCh37.p13 chr8: 446,129-5,976,513 LOC105377795, LOC100131395, 47 more genes
    nsv7064753inversion1nstd229human GRCh38 chr8: 1,861,030-2,080,723 , GRCh37.p13 chr8: 1,809,196-1,965,389 ARHGEF10, LOC100131395, 5 more genes
    nsv7062154inversion1nstd229human GRCh38 chr8: 1,744,685-2,489,179 , GRCh37.p13 chr8: 1,692,851-2,346,295 LOC105377782, KBTBD11, 15 more genes
    nsv7061516inversion1nstd229human GRCh38 chr8: 2,114,515-2,119,799 , GRCh37.p13 chr8|NW_003571042.1: 96,917-102,199 MYOM2
    nsv7059901inversion1nstd229human GRCh37.p13 chr8|NW_003571042.1: 8,467-324,019 , GRCh38 chr8: 2,025,693-2,486,122 LOC105377782, LOC105377783, 4 more genes
    nsv7059889inversion1nstd229human GRCh38 chr8: 1,445,340-4,898,472 , GRCh37.p13 chr8: 1,393,506-4,755,994 LOC105377790, RNA5SP251, 27 more genes
    nsv7059594inversion1nstd229human GRCh38 chr8: 441,112-6,103,891 , GRCh37.p13 chr8: 391,112-5,961,413 LOC286083, MIR3674, 48 more genes
    nsv6857658copy number variation1nstd229human GRCh38 chr8: 2,113,097-2,142,308 , GRCh37.p13 chr8|NW_003571042.1: 95,499-124,844 MYOM2
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