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Items: 1 to 20 of 460

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140993copy number variation1nstd232human GRCh37.p13 chrX: 114,360,011-114,360,136 , GRCh38.p12 chrX: 115,125,448-115,125,573 LRCH2, SNORA35B
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7082786copy number variation1nstd229human GRCh38 chrX: 115,173,425-115,182,573 , GRCh37.p13 chrX|NW_004070891.1: 842,227-851,375 , GRCh37.p13 chrX: 114,407,988-114,417,136 LRCH2
    nsv7082785copy number variation1nstd229human GRCh38 chrX: 115,165,301-115,166,020 , GRCh37.p13 chrX|NW_004070891.1: 834,103-834,822 , GRCh37.p13 chrX: 114,399,864-114,400,583 LRCH2
    nsv7082784copy number variation1nstd229human GRCh38 chrX: 115,164,401-115,166,200 , GRCh37.p13 chrX: 114,398,964-114,400,763 , GRCh37.p13 chrX|NW_004070891.1: 833,203-835,002 LRCH2
    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
    nsv7082782copy number variation1nstd229human GRCh38 chrX: 115,133,497-115,133,647 , GRCh37.p13 chrX|NW_004070891.1: 802,299-802,449 , GRCh37.p13 chrX: 114,368,060-114,368,210 TMSB4XP7, LRCH2
    nsv7082781copy number variation1nstd229human GRCh38 chrX: 115,129,805-115,130,193 , GRCh37.p13 chrX|NW_004070891.1: 798,607-798,995 , GRCh37.p13 chrX: 114,364,368-114,364,756 LRCH2
    nsv7082780copy number variation1nstd229human GRCh38 chrX: 115,108,980-115,109,052 , GRCh37.p13 chrX|NW_004070891.1: 777,782-777,854 , GRCh37.p13 chrX: 114,343,543-114,343,615 LRCH2
    nsv7082774copy number variation1nstd229human GRCh38 chrX: 115,043,024-115,141,940 , GRCh37.p13 chrX|NW_004070891.1: 711,826-810,742 , GRCh37.p13 chrX: 114,277,587-114,376,503 TMSB4XP7, YAP1P2, 3 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
    nsv7082766copy number variation1nstd229human GRCh38 chrX: 114,967,276-115,163,566 , GRCh37.p13 chrX|NW_004070891.1: 636,078-832,368 , GRCh37.p13 chrX: 114,201,839-114,398,129 LRCH2, RNU6-648P, 5 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
    nsv7040560inversion1nstd229human GRCh38 chrX: 115,146,377-115,146,404 , GRCh37.p13 chrX|NW_004070891.1: 815,179-815,206 , GRCh37.p13 chrX: 114,380,940-114,380,967 LRCH2
    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
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