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Items: 1 to 20 of 445

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148062copy number variation1nstd102humanPathogenic GRCh37 chrX: 53,239,546-53,349,064 , GRCh38.p12 chrX: 53,210,364-53,319,866 IQSEC2, KDM5C
    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
    nsv7098562copy number variation1nstd102humanPathogenic GRCh37 chrX: 53,263,401-53,280,376 , GRCh38.p12 chrX: 53,234,219-53,251,194 IQSEC2
    nsv7098538copy number variation1nstd102humanLikely benign GRCh37 chrX: 53,349,595-53,571,743 , GRCh38.p12 chrX: 53,320,397-53,544,782 SMC1A, HSD17B10, 8 more genes
    nsv7098537copy number variation1nstd102humanUncertain significance GRCh37 chrX: 53,272,494-53,461,292 , GRCh38.p12 chrX: 53,243,312-53,434,345 RIBC1, MPV17L2P1, 5 more genes
    nsv7098536copy number variation1nstd102humanUncertain significance GRCh37 chrX: 53,222,149-53,622,383 , GRCh38.p12 chrX: 53,192,967-53,595,423 KDM5C, RIBC1, 13 more genes
    nsv7098535copy number variation1nstd102humanUncertain significance GRCh37 chrX: 53,222,149-53,461,292 , GRCh38.p12 chrX: 53,192,967-53,434,345 KDM5C, RIBC1, 8 more genes
    nsv7098323copy number variation1nstd102humanPathogenic GRCh37 chrX: 53,222,149-55,057,617 , GRCh38.p12 chrX: 53,192,967-55,031,184 RPL37P24, KDM5C, 34 more genes
    nsv7091839copy number variation1nstd229human GRCh38 chrX: 53,289,895-53,291,178 , GRCh37.p13 chrX: 53,319,077-53,320,360 , GRCh37.p13 chrX|NW_004070877.1: 3,003,010-3,004,293 IQSEC2
    nsv7091838copy number variation1nstd229human GRCh38 chrX: 53,289,001-53,442,000 , GRCh37.p13 chrX|NW_004070877.1: 3,002,116-3,155,115 , GRCh37.p13 chrX: 53,318,183-53,468,947 SMC1A, HSD17B10, 5 more genes
    nsv7091837copy number variation1nstd229human GRCh38 chrX: 53,288,998-53,450,810 , GRCh37.p13 chrX|NW_004070877.1: 3,002,113-3,163,925 , GRCh37.p13 chrX: 53,318,180-53,477,758 RIBC1, IQSEC2, 5 more genes
    nsv7091836copy number variation1nstd229human GRCh38 chrX: 53,284,454-53,284,746 , GRCh37.p13 chrX|NW_004070877.1: 2,997,569-2,997,861 , GRCh37.p13 chrX: 53,313,636-53,313,928 IQSEC2
    nsv7091835copy number variation1nstd229human GRCh38 chrX: 53,283,342-53,283,376 , GRCh37.p13 chrX|NW_004070877.1: 2,996,457-2,996,491 , GRCh37.p13 chrX: 53,312,524-53,312,558 IQSEC2
    nsv7091834copy number variation1nstd229human GRCh38 chrX: 53,259,596-53,259,730 , GRCh37.p13 chrX|NW_004070877.1: 2,972,711-2,972,845 , GRCh37.p13 chrX: 53,288,778-53,288,912 IQSEC2
    nsv7091833copy number variation1nstd229human GRCh38 chrX: 53,258,424-53,273,527 , GRCh37.p13 chrX: 53,287,606-53,302,709 , GRCh37.p13 chrX|NW_004070877.1: 2,971,539-2,986,642 IQSEC2
    nsv7091832copy number variation1nstd229human GRCh38 chrX: 53,243,620-53,462,258 , GRCh37.p13 chrX: 53,272,802-53,489,199 , GRCh37.p13 chrX|NW_004070877.1: 2,956,735-3,175,373 MIR6857, RIBC1, 7 more genes
    nsv7091831copy number variation1nstd229human GRCh38 chrX: 53,233,901-53,311,900 , GRCh37.p13 chrX|NW_004070877.1: 2,947,016-3,025,015 , GRCh37.p13 chrX: 53,263,083-53,341,098 IQSEC2
    nsv7091830copy number variation1nstd229human GRCh38 chrX: 53,225,624-53,234,508 , GRCh37.p13 chrX|NW_004070877.1: 2,938,739-2,947,623 , GRCh37.p13 chrX: 53,254,806-53,263,690 KDM5C, IQSEC2
    nsv7091829copy number variation1nstd229human GRCh38 chrX: 53,224,901-53,320,600 , GRCh37.p13 chrX: 53,254,083-53,349,798 , GRCh37.p13 chrX|NW_004070877.1: 2,938,016-3,033,715 KDM5C, IQSEC2
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