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Items: 1 to 20 of 376

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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
    nsv7082793copy number variation1nstd229human GRCh38 chrX: 115,307,890-115,309,949 , GRCh37.p13 chrX|NW_004070891.1: 976,692-978,751 , GRCh37.p13 chrX: 114,542,455-114,544,514 LUZP4
    nsv7082792copy number variation1nstd229human GRCh38 chrX: 115,307,556-115,310,018 , GRCh37.p13 chrX: 114,542,121-114,544,583 , GRCh37.p13 chrX|NW_004070891.1: 976,358-978,820 LUZP4
    nsv7082791copy number variation1nstd229human GRCh38 chrX: 115,305,420-115,627,472 , GRCh37.p13 chrX|NW_004070891.1: 974,222-1,296,274 , GRCh37.p13 chrX: 114,539,985-114,861,784 LOC105373314, PLS3, 4 more genes
    nsv7082790copy number variation1nstd229human GRCh38 chrX: 115,299,661-115,357,567 , GRCh37.p13 chrX|NW_004070891.1: 968,463-1,026,369 , GRCh37.p13 chrX: 114,534,227-114,592,213 LOC107985681, LUZP4
    nsv7082789copy number variation1nstd229human GRCh38 chrX: 115,291,939-115,292,147 , GRCh37.p13 chrX|NW_004070891.1: 960,741-960,949 , GRCh37.p13 chrX: 114,526,505-114,526,713 LUZP4
    nsv7082783copy number variation1nstd229human GRCh38 chrX: 115,144,540-115,620,007 , GRCh37.p13 chrX|NW_004070891.1: 813,342-1,288,809 , GRCh37.p13 chrX: 114,379,103-114,854,319 LOC107985681, LRCH2, 7 more genes
    nsv7082769copy number variation1nstd229human GRCh38 chrX: 115,008,958-115,349,261 , GRCh37.p13 chrX|NW_004070891.1: 677,760-1,018,063 , GRCh37.p13 chrX: 114,243,521-114,583,909 RBMXL3, SNORA35B, 9 more genes
    nsv7082752copy number variation1nstd229human GRCh38 chrX: 114,787,493-115,300,260 , GRCh37.p13 chrX|NW_004070891.1: 456,295-969,062 , GRCh37.p13 chrX: 114,022,056-114,534,826 LOC105373313, LRCH2, 11 more genes
    nsv7055271inversion1nstd229human GRCh38 chrX: 114,091,775-119,749,531 , GRCh37.p13 chrX: 115,732,291-118,883,494 ZCCHC12, CT47C1, 83 more genes
    nsv7053216inversion1nstd229human GRCh38 chrX: 114,054,506-118,815,100 , GRCh37.p13 chrX: 113,297,697-115,918,761 LUZP4, LOC107985681, 57 more genes
    nsv7048914inversion1nstd229human GRCh38 chrX: 113,754,776-118,814,265 , GRCh37.p13 chrX: 112,998,052-115,918,761 RN7SL712P, SLC6A14, 61 more genes
    nsv7048750inversion1nstd229human GRCh38 chrX: 114,054,489-118,815,074 , GRCh37.p13 chrX: 113,297,680-115,918,761 CT83, MIR1912, 57 more genes
    nsv7048375inversion1nstd229human GRCh38 chrX: 113,143,339-118,246,278 , GRCh37.p13 chrX: 112,386,567-117,380,241 RNU6-154P, HSPA8P7, 58 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
    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
    nsv6633750copy number variation1nstd224human GRCh37 chrX: 114,524,333-114,546,062 , GRCh38.p12 chrX: 115,289,767-115,311,495 LUZP4
    nsv6633565copy number variation1nstd224human GRCh37 chrX: 107,804,808-114,879,367 , GRCh38.p12 chrX: 108,561,578-115,645,047 DCX, IL13RA2, 80 more genes
    nsv6315429copy number variation1nstd102humanPathogenic GRCh37 chrX: 77,670,699-155,233,731 , GRCh38.p12 chrX: 78,415,202-156,004,066 H2AB1, GPR174, 1081 more genes
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