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Items: 1 to 20 of 875

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138253copy number variation1nstd232human GRCh37.p13 chrX: 114,041,658-114,041,744 , GRCh38.p12 chrX: 114,807,095-114,807,181 HTR2C, LOC105373313
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7082759copy number variation1nstd229human GRCh38 chrX: 114,908,198-114,919,211 , GRCh37.p13 chrX|NW_004070891.1: 577,000-588,013 , GRCh37.p13 chrX: 114,142,761-114,153,774 HTR2C
    nsv7082758copy number variation1nstd229human GRCh38 chrX: 114,907,941-114,954,883 , GRCh37.p13 chrX|NW_004070891.1: 576,743-623,685 , GRCh37.p13 chrX: 114,142,504-114,189,446 HTR2C
    nsv7082757copy number variation1nstd229human GRCh38 chrX: 114,899,664-114,899,748 , GRCh37.p13 chrX: 114,134,227-114,134,311 , GRCh37.p13 chrX|NW_004070891.1: 568,466-568,550 HTR2C
    nsv7082756copy number variation1nstd229human GRCh38 chrX: 114,871,601-114,881,100 , GRCh37.p13 chrX|NW_004070891.1: 540,403-549,902 , GRCh37.p13 chrX: 114,106,164-114,115,663 HTR2C
    nsv7082755copy number variation1nstd229human GRCh38 chrX: 114,837,224-114,837,664 , GRCh37.p13 chrX|NW_004070891.1: 506,026-506,466 , GRCh37.p13 chrX: 114,071,787-114,072,227 HTR2C
    nsv7082754copy number variation1nstd229human GRCh38 chrX: 114,818,301-114,822,100 , GRCh37.p13 chrX|NW_004070891.1: 487,103-490,902 , GRCh37.p13 chrX: 114,052,864-114,056,663 MIR448, HTR2C
    nsv7082753copy number variation1nstd229human GRCh38 chrX: 114,791,850-114,809,423 , GRCh37.p13 chrX: 114,026,413-114,043,986 , GRCh37.p13 chrX|NW_004070891.1: 460,652-478,225 LOC105373313, HTR2C
    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
    nsv7082751copy number variation1nstd229human GRCh38 chrX: 114,783,988-115,043,061 , GRCh37.p13 chrX: 114,018,551-114,277,624 , GRCh37.p13 chrX|NW_004070891.1: 452,790-711,863 IL13RA2, HTR2C, 3 more genes
    nsv7082750copy number variation1nstd229human GRCh38 chrX: 114,769,439-114,769,498 , GRCh37.p13 chrX|NW_004070891.1: 438,241-438,300 , GRCh37.p13 chrX: 114,003,992-114,004,051 LOC105373313, HTR2C
    nsv7082749copy number variation1nstd229human GRCh38 chrX: 114,745,868-115,056,259 , GRCh37.p13 chrX|NW_004070891.1: 414,670-725,061 , GRCh37.p13 chrX: 113,980,307-114,290,822 HTR2C, IL13RA2, 5 more genes
    nsv7082748copy number variation1nstd229human GRCh38 chrX: 114,744,663-114,778,448 , GRCh37.p13 chrX|NW_004070891.1: 413,465-447,250 , GRCh37.p13 chrX: 113,979,102-114,013,007 MIR1911, HSPA8P7, 2 more genes
    nsv7082747copy number variation1nstd229human GRCh38 chrX: 114,704,438-114,712,851 , GRCh37.p13 chrX|NW_004070891.1: 373,240-381,653 , GRCh37.p13 chrX: 113,938,854-113,947,268 HTR2C
    nsv7082746copy number variation1nstd229human GRCh38 chrX: 114,696,001-114,706,800 , GRCh37.p13 chrX|NW_004070891.1: 364,803-375,602 , GRCh37.p13 chrX: 113,930,433-113,941,215 HTR2C
    nsv7082745copy number variation1nstd229human GRCh38 chrX: 114,678,101-114,696,300 , GRCh37.p13 chrX|NW_004070891.1: 346,903-365,102 , GRCh37.p13 chrX: 113,912,577-113,930,732 HTR2C
    nsv7082744copy number variation1nstd229human GRCh38 chrX: 114,669,618-114,672,687 , GRCh37.p13 chrX|NW_004070891.1: 338,420-341,489 , GRCh37.p13 chrX: 113,904,097-113,907,163 HTR2C
    nsv7082743copy number variation1nstd229human GRCh38 chrX: 114,666,501-114,696,400 , GRCh37.p13 chrX: 113,900,980-113,930,832 , GRCh37.p13 chrX|NW_004070891.1: 335,303-365,202 HTR2C
    nsv7082742copy number variation1nstd229human GRCh38 chrX: 114,659,263-114,883,869 , GRCh37.p13 chrX|NW_004070891.1: 328,065-552,671 , GRCh37.p13 chrX: 113,893,740-114,118,432 MIR448, HTR2C, 4 more genes
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