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Items: 1 to 20 of 439

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098592copy number variation3nstd102humanPathogenic, Uncertain significance GRCh37 chrX: 14,861,689-15,870,650 , GRCh38.p12 chrX: 14,843,567-15,852,527 VEGFD, CA5BP1-CA5B, 20 more genes
    nsv7085473copy number variation1nstd229human GRCh38 chrX: 15,265,887-15,855,049 , GRCh37.p13 chrX: 15,284,009-15,873,172 CLTRN, ZRSR2, 16 more genes
    nsv7085472copy number variation1nstd229human GRCh38 chrX: 15,260,411-15,260,795 , GRCh37.p13 chrX: 15,278,533-15,278,917 ASB9
    nsv7085471copy number variation1nstd229human GRCh38 chrX: 15,254,418-15,254,687 , GRCh37.p13 chrX: 15,272,540-15,272,809 ASB9
    nsv7085470copy number variation1nstd229human GRCh38 chrX: 15,246,901-15,271,500 , GRCh37.p13 chrX: 15,265,023-15,289,622 ASB9
    nsv7085466copy number variation1nstd229human GRCh38 chrX: 15,205,544-15,274,264 , GRCh37.p13 chrX: 15,223,666-15,292,386 ASB9
    nsv7085463copy number variation1nstd229human GRCh38 chrX: 15,192,575-15,841,474 , GRCh37.p13 chrX: 15,210,697-15,859,597 CA5B, AP1S2, 16 more genes
    nsv7085455copy number variation1nstd229human GRCh38 chrX: 15,114,392-15,534,944 , GRCh37.p13 chrX: 15,132,514-15,553,067 ACE2, PIR-FIGF, 7 more genes
    nsv7085443copy number variation1nstd229human GRCh38 chrX: 15,075,262-15,384,610 , GRCh37.p13 chrX: 15,093,384-15,402,732 PIR, RPL35AP37, 5 more genes
    nsv7085015copy number variation1nstd229human GRCh38 chrX: 14,650,010-15,265,016 , GRCh37.p13 chrX: 14,668,132-15,283,138 MOSPD2, ASB9, 5 more genes
    nsv7037021inversion1nstd229human GRCh38 chrX: 14,941,162-18,599,007 , GRCh37.p13 chrX: 14,959,284-18,617,127 TXLNG, MIR4768, 54 more genes
    nsv7032726inversion1nstd229human GRCh38 chrX: 14,932,558-15,874,827 , GRCh37.p13 chrX: 14,950,680-15,892,950 INE2, HNRNPDLP5, 18 more genes
    nsv7023785inversion1nstd229human GRCh38 chrX: 13,472,327-15,761,537 , GRCh37.p13 chrX: 13,490,446-15,779,660 MIR6086, ACE2, 33 more genes
    nsv7021157inversion1nstd229human GRCh38 chrX: 14,244,684-19,508,867 , GRCh37.p13 chrX: 14,262,806-19,526,985 CA5BP1, CDKL5, 74 more genes
    nsv6636009copy number variation1nstd102humanUncertain significance GRCh37 chrX: 14,644,702-15,779,774 , GRCh38.p12 chrX: 14,626,580-15,761,651 ACE2-DT, PIGA, 19 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6634135copy number variation1nstd224human GRCh37 chrX: 2,700,157-26,836,730 , GRCh38.p12 chrX: 2,782,116-26,818,613 AMELX, ARSF, 258 more genes
    nsv6634127copy number variation1nstd224human GRCh37 chrX: 15,172,189-15,867,450 , GRCh38.p12 chrX: 15,154,067-15,849,327 CLTRN, ACE2-DT, 16 more genes
    nsv6315577complex substitution1nstd102humanPathogenic GRCh37 chrX: 590,376-56,315,041 , GRCh38.p12 chrX: 629,641-56,288,608 ACTG1P10, NR0B1, 778 more genes
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