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Items: 1 to 20 of 375

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137157inversion1nstd234human GRCh37 chrX: 31,626,542-82,320,140 , GRCh38.p12 chrX: 31,608,425-83,065,132 ABCB7, ACTG1P10, 775 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098530copy number variation1nstd102humanUncertain significance GRCh37 chrX: 40,440,318-41,782,241 , GRCh38.p12 chrX: 40,581,066-41,922,988 RN7SL144P, TNIP2P1, 27 more genes
    nsv7098307copy number variation3nstd102humanPathogenic, Uncertain significance GRCh37 chrX: 39,911,362-41,782,241 , GRCh38.p12 chrX: 40,052,109-41,922,988 LOC107985687, BCOR, 33 more genes
    nsv7081031copy number variation1nstd229human GRCh38 chrX: 40,645,935-40,646,260 , GRCh37.p13 chrX: 40,505,187-40,505,512 CXorf38
    nsv7081030copy number variation1nstd229human GRCh38 chrX: 40,634,242-40,634,416 , GRCh37.p13 chrX: 40,493,494-40,493,668 CXorf38
    nsv7081029copy number variation1nstd229human GRCh38 chrX: 40,631,760-40,632,698 , GRCh37.p13 chrX: 40,491,012-40,491,950 CXorf38
    nsv7081028copy number variation1nstd229human GRCh38 chrX: 40,631,301-40,632,600 , GRCh37.p13 chrX: 40,490,553-40,491,852 CXorf38
    nsv7081027copy number variation1nstd229human GRCh38 chrX: 40,615,160-40,942,802 , GRCh37.p13 chrX: 40,474,412-40,802,055 TNIP2P1, MED14, 9 more genes
    nsv7081026copy number variation1nstd229human GRCh38 chrX: 40,612,385-40,627,356 , GRCh37.p13 chrX: 40,471,637-40,486,608 MPC1L, CXorf38
    nsv7081015copy number variation1nstd229human GRCh38 chrX: 40,514,624-40,632,421 , GRCh37.p13 chrX: 40,373,876-40,491,673 CXorf38, MPC1L, 2 more genes
    nsv7081009copy number variation1nstd229human GRCh38 chrX: 40,487,001-41,078,400 , GRCh37.p13 chrX: 40,346,253-40,937,653 CXorf38, MPC1L, 12 more genes
    nsv7081006copy number variation1nstd229human GRCh38 chrX: 40,468,161-40,690,469 , GRCh37.p13 chrX: 40,327,413-40,549,721 RNU7-164P, ATP6AP2, 3 more genes
    nsv7080987copy number variation1nstd229human GRCh38 chrX: 40,279,104-40,632,084 , GRCh37.p13 chrX: 40,138,357-40,491,336 RNU7-164P, ATP6AP2, 5 more genes
    nsv7080985copy number variation1nstd229human GRCh38 chrX: 40,263,272-41,326,727 , GRCh37.p13 chrX: 40,122,525-41,185,980 CLIC4P3, MPC1L, 19 more genes
    nsv7080971copy number variation1nstd229human GRCh38 chrX: 40,188,484-41,072,065 , GRCh37.p13 chrX: 40,047,737-40,931,318 CXorf38, MPC1L, 14 more genes
    nsv7033650inversion1nstd229human GRCh38 chrX: 37,770,465-43,935,549 , GRCh37.p13 chrX: 37,669,767-43,794,795 RN7SL15P, NANOGP10, 79 more genes
    nsv7032924inversion1nstd229human GRCh38 chrX: 34,355,734-41,258,887 , GRCh37.p13 chrX: 34,373,851-41,118,140 IMPDH1P2, RPL32P36, 81 more genes
    nsv6637069copy number variation1nstd102humanPathogenic GRCh37 chrX: 39,525,562-52,832,596 , GRCh38.p12 chrX: 39,666,308-52,803,572 LOC100419238, NDP, 312 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
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