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Items: 1 to 20 of 332

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147750insertion1nstd232human GRCh37.p13 chrX: 84,009,827-84,009,827 , GRCh38.p12 chrX: 84,754,819-84,754,819 SETP4, TEX16P
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7089980copy number variation1nstd229human GRCh38 chrX: 84,749,690-84,756,509 , GRCh37.p13 chrX: 84,004,698-84,011,517 SETP4, TEX16P
    nsv7089978copy number variation1nstd229human GRCh38 chrX: 84,722,029-85,127,087 , GRCh37.p13 chrX: 83,977,037-84,382,093 SETP4, TEX16P, 3 more genes
    nsv7089977copy number variation1nstd229human GRCh38 chrX: 84,715,034-85,127,086 , GRCh37.p13 chrX: 83,970,042-84,382,092 APOOL, TEX16P, 3 more genes
    nsv7089976copy number variation1nstd229human GRCh38 chrX: 84,700,758-84,800,864 , GRCh37.p13 chrX: 83,955,766-84,055,871 SETP4, TEX16P
    nsv7089972copy number variation1nstd229human GRCh38 chrX: 84,676,727-85,239,427 , GRCh37.p13 chrX: 83,931,735-84,494,433 TEX16P, UBE2DNL, 4 more genes
    nsv7089968copy number variation1nstd229human GRCh38 chrX: 84,637,690-84,779,622 , GRCh37.p13 chrX: 83,892,698-84,034,629 SETP4, TEX16P
    nsv7089963copy number variation1nstd229human GRCh38 chrX: 84,587,230-84,812,571 , GRCh37.p13 chrX: 83,842,238-84,067,578 SETP4, TEX16P
    nsv7089961copy number variation1nstd229human GRCh38 chrX: 84,577,647-84,793,855 , GRCh37.p13 chrX: 83,832,655-84,048,862 SETP4, TEX16P
    nsv7089949copy number variation1nstd229human GRCh38 chrX: 84,472,787-84,939,908 , GRCh37.p13 chrX: 83,727,795-84,194,914 SETP4, HDX, 2 more genes
    nsv7089938copy number variation1nstd229human GRCh38 chrX: 84,344,651-85,139,490 , GRCh37.p13 chrX: 83,599,659-84,394,496 HDX, SETP4, 4 more genes
    nsv7089888copy number variation1nstd229human GRCh38 chrX: 84,049,002-84,793,601 , GRCh37.p13 chrX: 83,304,010-84,048,608 RPS6KA6, SETP4, 3 more genes
    nsv7055601inversion1nstd229human GRCh38 chrX: 84,756,374-84,762,069 , GRCh37.p13 chrX: 84,011,382-84,017,077 SETP4, TEX16P
    nsv7047022inversion1nstd229human GRCh38 chrX: 84,510,618-84,800,824 , GRCh37.p13 chrX: 83,765,626-84,055,831 SETP4, TEX16P
    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
    nsv6634176copy number variation1nstd224human GRCh37 chrX: 83,658,710-84,394,032 , GRCh38.p12 chrX: 84,403,702-85,139,026 APOOL, HDX, 4 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
    nsv6315393copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,545-155,226,048 , GRCh38.p12 chrX: 11,545-155,996,383 H2BP8, LOC101060199, 2151 more genes
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