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Items: 1 to 20 of 298

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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
    nsv7087400copy number variation1nstd229human GRCh38 chrX: 42,670,948-42,878,879 , GRCh37.p13 chrX: 42,530,199-42,738,128 LOC105373186, PPP1R2C
    nsv7087396copy number variation1nstd229human GRCh38 chrX: 42,647,876-42,958,385 , GRCh37.p13 chrX: 42,507,128-42,817,634 PPP1R2C, LOC105373188, 1 more genes
    nsv7087395copy number variation1nstd229human GRCh38 chrX: 42,646,598-42,958,384 , GRCh37.p13 chrX: 42,505,850-42,817,633 LOC105373188, LOC105373186, 1 more genes
    nsv7087379copy number variation1nstd229human GRCh38 chrX: 42,459,670-43,102,685 , GRCh37.p13 chrX: 42,318,922-42,961,934 LOC105373186, PPP1R2C, 3 more genes
    nsv7087375copy number variation1nstd229human GRCh38 chrX: 42,398,311-43,026,850 , GRCh37.p13 chrX: 42,257,563-42,886,099 PPP1R2C, LOC105373188, 3 more genes
    nsv7036033inversion1nstd229human GRCh38 chrX: 41,966,468-43,384,957 , GRCh37.p13 chrX: 41,825,721-43,244,206 ATP5MC2P4, LOC105373186, 8 more genes
    nsv7034675inversion1nstd229human GRCh38 chrX: 42,652,466-43,294,602 , GRCh37.p13 chrX: 42,511,718-43,153,851 LOC105373186, SMIM15P1, 4 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
    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
    nsv6636868copy number variation1nstd102humanUncertain significance GRCh37 chrX: 42,327,130-42,807,122 , GRCh38.p12 chrX: 42,467,878-42,947,873 LOC112268309, LOC105373188, 2 more genes
    nsv6636684copy number variation1nstd102humanPathogenic GRCh37 chrX: 41,350,855-44,616,591 , GRCh38.p12 chrX: 41,491,602-44,757,345 PINCR, YWHAZP10, 31 more genes
    nsv6634252copy number variation1nstd224human GRCh37 chrX: 42,337,775-42,707,170 , GRCh38.p12 chrX: 42,478,523-42,847,920 PPP1R2C, LOC112268309, 1 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6315577complex substitution1nstd102humanPathogenic GRCh37 chrX: 590,376-56,315,041 , GRCh38.p12 chrX: 629,641-56,288,608 ACTG1P10, NR0B1, 778 more genes
    nsv6315393copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,545-155,226,048 , GRCh38.p12 chrX: 11,545-155,996,383 H2BP8, LOC101060199, 2151 more genes
    nsv6315389copy number variation1nstd102humanPathogenic GRCh37 chrX: 11,522,765-155,233,731 , GRCh38.p12 chrX: 11,504,645-156,004,066 RBMX, LOC100129144, 2042 more genes
    nsv6315331copy number variation4nstd102humanPathogenic GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 PLAC1, PGK1P1, 2154 more genes
    nsv6315330copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-57,841,304 , GRCh38.p12 chrX: 251,879-57,814,871 NPM1P9, UBE2E4P, 799 more genes
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