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Items: 1 to 20 of 384

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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
    nsv7090681copy number variation1nstd229human GRCh38 chrX: 104,135,907-104,136,586 , GRCh37.p13 chrX|NW_004070885.1: 272,323-273,002 , GRCh37.p13 chrX: 103,380,588-103,381,267 SLC25A53
    nsv7090680copy number variation1nstd229human GRCh38 chrX: 104,135,701-104,152,600 , GRCh37.p13 chrX|NW_004070885.1: 272,117-289,016 , GRCh37.p13 chrX: 103,380,382-103,397,281 SLC25A53
    nsv7090679copy number variation1nstd229human GRCh38 chrX: 104,134,150-104,137,605 , GRCh37.p13 chrX|NW_004070885.1: 270,566-274,021 , GRCh37.p13 chrX: 103,378,831-103,382,286 SLC25A53
    nsv7090678copy number variation1nstd229human GRCh38 chrX: 104,133,369-104,133,787 , GRCh37.p13 chrX|NW_004070885.1: 269,785-270,203 , GRCh37.p13 chrX: 103,378,050-103,378,468 SLC25A53
    nsv7090677copy number variation1nstd229human GRCh38 chrX: 104,129,001-104,139,200 , GRCh37.p13 chrX|NW_004070885.1: 265,417-275,616 , GRCh37.p13 chrX: 103,373,684-103,383,881 SLC25A53
    nsv7090676copy number variation1nstd229human GRCh38 chrX: 104,124,117-104,152,913 , GRCh37.p13 chrX|NW_004070885.1: 260,533-289,329 , GRCh37.p13 chrX: 103,368,802-103,397,594 SLC25A53, LOC286437
    nsv7090675copy number variation1nstd229human GRCh38 chrX: 104,120,852-104,124,591 , GRCh37.p13 chrX|NW_004070885.1: 257,268-261,007 , GRCh37.p13 chrX: 103,365,543-103,369,276 LOC286437, ZCCHC18, 1 more genes
    nsv7090674copy number variation1nstd229human GRCh38 chrX: 104,107,605-104,107,624 , GRCh37.p13 chrX|NW_004070885.1: 244,021-244,040 , GRCh37.p13 chrX: 103,352,288-103,352,307 SLC25A53
    nsv7090673copy number variation1nstd229human GRCh38 chrX: 104,106,797-104,106,877 , GRCh37.p13 chrX: 103,351,480-103,351,560 , GRCh37.p13 chrX|NW_004070885.1: 243,213-243,293 SLC25A53
    nsv7090672copy number variation1nstd229human GRCh38 chrX: 104,106,401-104,108,000 , GRCh37.p13 chrX|NW_004070885.1: 242,817-244,416 , GRCh37.p13 chrX: 103,351,084-103,352,683 SLC25A53
    nsv7056502inversion1nstd229human GRCh38 chrX: 103,955,056-104,169,610 , GRCh37.p13 chrX|NW_004070885.1: 91,472-306,026 , GRCh37.p13 chrX: 103,209,629-103,414,291 H2BW4P, SLC25A53, 11 more genes
    nsv7052699inversion1nstd229human GRCh38 chrX: 104,119,257-104,119,288 , GRCh37.p13 chrX: 103,363,948-103,363,979 , GRCh37.p13 chrX|NW_004070885.1: 255,673-255,704 ZCCHC18, SLC25A53
    nsv7052621inversion1nstd229human GRCh38 chrX: 103,826,879-110,334,422 , GRCh37.p13 chrX: 103,081,809-109,577,650 CSGALNACT2P2, LOC107985662, 82 more genes
    nsv7051544inversion1nstd229human GRCh38 chrX: 104,135,721-104,156,843 , GRCh37.p13 chrX: 103,380,402-103,401,524 , GRCh37.p13 chrX|NW_004070885.1: 272,137-293,259 SLC25A53
    nsv7046335inversion1nstd229human GRCh37.p13 chrX|NW_004070885.1: 136,840-262,344 , GRCh38 chrX: 104,000,424-104,125,928 , GRCh37.p13 chrX: 103,254,996-103,370,611 DPPA3P4, H2BW1, 6 more genes
    nsv7045046inversion1nstd229human GRCh38 chrX: 104,156,130-104,161,859 , GRCh37.p13 chrX: 103,400,811-103,406,540 , GRCh37.p13 chrX|NW_004070885.1: 292,546-298,275 SLC25A53
    nsv7038256inversion1nstd229human GRCh38 chrX: 103,921,291-104,110,334 , GRCh37.p13 chrX: 103,175,874-103,355,025 , GRCh37.p13 chrX|NW_004070885.1: 57,707-246,750 SLC25A53, H2BW4P, 9 more genes
    nsv6636543copy number variation1nstd102humanPathogenic GRCh37 chrX: 93,805,850-118,913,329 , GRCh38.p12 chrX: 94,550,851-119,779,366 TRPC5OS, LOC105373314, 351 more genes
    nsv6634623copy number variation1nstd102humanPathogenic GRCh38 chrX: 103,776,506-104,817,980 , GRCh37.p13 chrX: 103,031,434-104,062,660 SLC25A53P1, ELF2P1, 22 more genes
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