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Items: 1 to 20 of 354

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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
    nsv7098786copy number variation1nstd102humanPathogenic GRCh37 chrX: 46,466,387-51,241,672 , GRCh38.p12 chrX: 46,606,952-51,498,820 LOC100419232, LOC791091, 172 more genes
    nsv7098417copy number variation2nstd102humanPathogenic GRCh37 chrX: 46,618,120-48,549,553 , GRCh38.p12 chrX: 46,758,685-48,691,162 ZNF81, LOC105373194, 84 more genes
    nsv7098318copy number variation3nstd102humanUncertain significance GRCh37 chrX: 47,001,716-50,659,607 , GRCh38.p12 chrX: 47,142,317-50,916,607 PYY3, CCDC120, 148 more genes
    nsv7098317copy number variation1nstd102humanPathogenic GRCh37 chrX: 46,466,387-50,659,607 , GRCh38.p12 chrX: 46,606,952-50,916,607 PLP2, RN7SL262P, 160 more genes
    nsv7087954copy number variation1nstd229human GRCh38 chrX: 48,338,448-48,348,591 , GRCh37.p13 chrX|NW_004070880.2: 577,877-588,020 , GRCh37.p13 chrX: 48,197,883-48,208,026 SSX3
    nsv7087952copy number variation1nstd229human GRCh38 chrX: 48,329,301-48,344,700 , GRCh37.p13 chrX|NW_004070880.2: 568,730-584,129 , GRCh37.p13 chrX: 48,188,736-48,204,135 SSX3, S100A11P9
    nsv7087889copy number variation1nstd229human GRCh38 chrX: 47,960,343-48,364,503 , GRCh37.p13 chrX|NW_004070880.2: 199,772-603,932 , GRCh37.p13 chrX: 47,819,742-48,223,938 S100A11P5, SSX9P, 24 more genes
    nsv7087888copy number variation1nstd229human GRCh38 chrX: 47,960,301-48,363,500 , GRCh37.p13 chrX|NW_004070880.2: 199,730-602,929 , GRCh37.p13 chrX: 47,819,700-48,222,935 SSX13P, LOC100420083, 24 more genes
    nsv7035366inversion1nstd229human GRCh38 chrX: 48,075,127-48,520,105 , GRCh37.p13 chrX|NW_004070880.2: 314,556-759,534 , GRCh37.p13 chrX: 47,934,496-48,378,493 S100A11P9, SSX4, 32 more genes
    nsv7034979inversion1nstd229human GRCh38 chrX: 46,796,509-48,396,328 , GRCh37.p13 chrX: 46,655,944-48,255,770 SSX1, S100A11P6, 66 more genes
    nsv7034533inversion1nstd229human GRCh38 chrX: 48,084,596-48,445,179 , GRCh37.p13 chrX|NW_004070880.2: 324,025-684,608 , GRCh37.p13 chrX: 47,943,965-48,303,559 RNU6-707P, SSX4, 27 more genes
    nsv7028188inversion1nstd229human GRCh38 chrX: 48,271,055-52,545,048 , GRCh37.p13 chrX|NW_004070877.1: 1-2,258,163 SSXP8, CACNA1F, 141 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
    nsv6634155copy number variation1nstd224human GRCh37 chrX: 47,970,653-48,219,069 , GRCh38.p12 chrX: 48,111,269-48,359,634 SSX5, LOC791091, 20 more genes
    nsv6634061copy number variation1nstd224human GRCh37 chrX: 48,117,179-48,219,069 , GRCh38.p12 chrX: 48,257,744-48,359,634 SSX3, SSXP8, 9 more genes
    nsv6634060copy number variation1nstd224human GRCh37 chrX: 47,911,871-48,205,223 , GRCh38.p12 chrX: 48,052,481-48,345,788 ZNF630, SSX13P, 21 more genes
    nsv6633880copy number variation1nstd224human GRCh37 chrX: 48,003,920-48,219,069 , GRCh38.p12 chrX: 48,144,492-48,359,634 SSX5, SSX19P, 18 more genes
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