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Items: 1 to 20 of 355

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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
    nsv7089235copy number variation1nstd229human GRCh38 chrX: 78,322,938-78,325,339 , GRCh37.p13 chrX: 77,578,435-77,580,836 CYSLTR1
    nsv7089234copy number variation1nstd229human GRCh38 chrX: 78,289,183-78,301,959 , GRCh37.p13 chrX: 77,544,680-77,557,456 CYSLTR1
    nsv7089233copy number variation1nstd229human GRCh38 chrX: 78,276,501-78,292,300 , GRCh37.p13 chrX: 77,531,998-77,547,797 CYSLTR1
    nsv7089232copy number variation1nstd229human GRCh38 chrX: 78,273,439-78,273,613 , GRCh37.p13 chrX: 77,528,936-77,529,110 CYSLTR1
    nsv7089231copy number variation1nstd229human GRCh38 chrX: 78,265,399-78,286,703 , GRCh37.p13 chrX: 77,520,896-77,542,200 CYSLTR1
    nsv7089230copy number variation1nstd229human GRCh38 chrX: 78,261,001-78,271,500 , GRCh37.p13 chrX: 77,516,498-77,526,997 CYSLTR1
    nsv7089223copy number variation1nstd229human GRCh38 chrX: 78,207,402-78,288,044 , GRCh37.p13 chrX: 77,462,899-77,543,541 CYSLTR1, LOC107985669
    nsv7089222copy number variation1nstd229human GRCh38 chrX: 78,194,995-78,394,988 , GRCh37.p13 chrX: 77,450,503-77,650,485 LOC107985669, CYSLTR1
    nsv7089218copy number variation1nstd229human GRCh38 chrX: 78,151,808-78,543,566 , GRCh37.p13 chrX: 77,450,503-77,799,063 FNDC3CP, HMGN1P34, 2 more genes
    nsv7033525inversion1nstd229human GRCh38 chrX: 77,852,956-78,523,514 , GRCh37.p13 chrX: 77,108,453-77,450,502 , GRCh37.p13 chrX|NW_003871101.3: 410,218-752,267 MAGT1, HMGN1P34, 10 more genes
    nsv7030871inversion1nstd229human GRCh38 chrX: 78,322,348-78,322,365 , GRCh37.p13 chrX: 77,577,845-77,577,862 CYSLTR1
    nsv7026063inversion1nstd229human GRCh38 chrX: 76,257,068-80,095,987 , GRCh37.p13 chrX: 75,477,467-77,450,502 ATRX, MAGEE1, 40 more genes
    nsv7025941inversion1nstd229human GRCh38 chrX: 78,302,305-78,328,981 , GRCh37.p13 chrX: 77,557,802-77,584,478 CYSLTR1
    nsv7021580inversion1nstd229human GRCh38 chrX: 78,299,464-78,317,402 , GRCh37.p13 chrX: 77,554,961-77,572,899 CYSLTR1
    nsv7018633inversion1nstd229human GRCh38 chrX: 76,256,859-80,096,106 , GRCh37.p13 chrX: 75,477,258-77,450,502 LDHBP2, ATP7A, 40 more genes
    nsv6636302copy number variation1nstd102humanUncertain significance GRCh37 chrX: 77,544,318-78,390,511 , GRCh38.p12 chrX: 78,288,821-79,135,014 HMGN1P34, CYSLTR1, 9 more genes
    nsv6634329copy number variation1nstd102humanPathogenic GRCh37 chrX: 76,794,355-119,282,836 , GRCh38.p12 chrX: 77,538,874-120,148,930 NXF4, RHOXF1P1, 489 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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