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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057933inversion1nstd229human GRCh38 chr7: 63,377,139-65,038,693 , GRCh37.p13 chr7: 62,837,517-64,499,071 , VN1R36P, 91 more genes
    nsv7055614inversion1nstd229human GRCh38 chr7: 63,982,028-64,332,022 , GRCh37.p13 chr7: 63,442,406-63,792,400 MTCO1P8, LOC105375322, 25 more genes
    nsv7053192inversion1nstd229human GRCh38 chr7: 63,873,376-64,215,440 , GRCh37.p13 chr7: 63,333,754-63,675,818 MTND4P2, LINC01005, 28 more genes
    nsv6836238copy number variation1nstd229human GRCh38 chr7: 64,019,170-64,034,488 , GRCh37.p13 chr7: 63,479,548-63,494,866 ZNF722, LINC01005, 1 more genes
    nsv6835588copy number variation1nstd229human GRCh38 chr7: 64,023,503-64,026,818 , GRCh37.p13 chr7: 63,483,881-63,487,196 LINC01005, ZNF722
    nsv6835251copy number variation1nstd229human GRCh38 chr7: 64,007,575-64,030,333 , GRCh37.p13 chr7: 63,467,953-63,490,711 LINC01005, LOC105375317, 1 more genes
    nsv6828632copy number variation1nstd229human GRCh38 chr7: 63,989,553-64,455,792 , GRCh37.p13 chr7: 63,449,931-63,916,170 MTCO2P8, MTND4P2, 29 more genes
    nsv6821711copy number variation1nstd229human GRCh38 chr7: 63,892,130-64,398,141 , GRCh37.p13 chr7: 63,352,508-63,858,519 ZNF722, LOC105375323, 36 more genes
    nsv6819370copy number variation1nstd229human GRCh38 chr7: 64,028,857-64,042,592 , GRCh37.p13 chr7: 63,489,235-63,502,970 LOC105375317, ZNF727, 1 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6632417copy number variation1nstd224human GRCh37 chr7: 63,352,782-63,962,963 , GRCh38.p12 chr7: 63,892,404-64,502,585 RPL6P20, ZNF680, 43 more genes
    nsv6632413copy number variation1nstd224human GRCh37 chr7: 62,241,041-64,438,809 , GRCh38.p12 chr7: 62,780,663-64,978,431 , ZNF138, 99 more genes
    nsv6618015copy number variation1nstd223human GRCh38 chr7: 64,029,689-64,295,968 , GRCh37.p13 chr7: 63,490,067-63,756,346 ZNF727, MTND4LP2, 22 more genes
    nsv6614052copy number variation1nstd223human GRCh38 chr7: 64,019,206-64,034,488 , GRCh37.p13 chr7: 63,479,584-63,494,866 LINC01005, LOC105375317, 1 more genes
    nsv6608686copy number variation1nstd223human GRCh38 chr7: 63,836,539-64,068,427 , GRCh37.p13 chr7: 63,296,917-63,528,805 , LOC107986731, 13 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6136196copy number variation1nstd213human GRCh37 chr7: 62,900,000-64,980,001 , GRCh38.p12 chr7: 63,439,622-65,515,088 , ZNF138, 95 more genes
    nsv6109072inversion1nstd212human GRCh37.p13 chr7: 63,442,406-63,526,518 , GRCh38 chr7: 63,982,028-64,066,140 ZNF727, ZNF722, 3 more genes
    nsv5927170copy number variation1nstd209human GRCh38 chr7: 64,022,336-64,278,876 , GRCh37.p13 chr7: 63,482,714-63,739,254 LOC105375317, ZNF735, 21 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
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