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Items: 1 to 20 of 441

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137157inversion1nstd234human GRCh37 chrX: 31,626,542-82,320,140 , GRCh38.p12 chrX: 31,608,425-83,065,132 ABCB7, ACTG1P10, 775 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098674copy number variation1nstd102humanPathogenic GRCh37 chrX: 73,744,174-73,749,296 , GRCh38.p12 chrX: 74,524,339-74,529,461 SLC16A2
    nsv7098567copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 73,641,473-74,376,107 , GRCh38.p12 chrX: 74,421,638-75,156,272 ABCB7, SLC16A2, 6 more genes
    nsv7092517copy number variation1nstd229human GRCh38 chrX: 74,530,527-74,530,860 , GRCh37.p13 chrX: 73,750,362-73,750,695 SLC16A2
    nsv7092516copy number variation1nstd229human GRCh38 chrX: 74,523,982-74,524,371 , GRCh37.p13 chrX: 73,743,817-73,744,206 SLC16A2
    nsv7092515copy number variation1nstd229human GRCh38 chrX: 74,520,781-74,520,883 , GRCh37.p13 chrX: 73,740,616-73,740,718 SLC16A2
    nsv7092514copy number variation1nstd229human GRCh38 chrX: 74,512,217-74,520,857 , GRCh37.p13 chrX: 73,732,052-73,740,692 SLC16A2
    nsv7092513copy number variation1nstd229human GRCh38 chrX: 74,493,773-74,559,735 , GRCh37.p13 chrX: 73,713,608-73,779,570 SLC16A2
    nsv7092512copy number variation1nstd229human GRCh38 chrX: 74,490,031-74,494,132 , GRCh37.p13 chrX: 73,709,866-73,713,967 SLC16A2
    nsv7092511copy number variation1nstd229human GRCh38 chrX: 74,486,580-74,486,925 , GRCh37.p13 chrX: 73,706,415-73,706,760 SLC16A2
    nsv7092510copy number variation1nstd229human GRCh38 chrX: 74,480,351-74,553,699 , GRCh37.p13 chrX: 73,700,186-73,773,534 SLC16A2
    nsv7092509copy number variation1nstd229human GRCh38 chrX: 74,472,179-74,488,861 , GRCh37.p13 chrX: 73,692,014-73,708,696 HNRNPA1P25, SLC16A2
    nsv7092508copy number variation1nstd229human GRCh38 chrX: 74,464,754-74,470,710 , GRCh37.p13 chrX: 73,684,589-73,690,545 SLC16A2, HNRNPA1P25
    nsv7092507copy number variation1nstd229human GRCh38 chrX: 74,430,101-74,434,900 , GRCh37.p13 chrX: 73,649,936-73,654,735 SLC16A2
    nsv7092506copy number variation1nstd229human GRCh38 chrX: 74,426,753-74,428,462 , GRCh37.p13 chrX: 73,646,588-73,648,297 SLC16A2
    nsv7092505copy number variation1nstd229human GRCh38 chrX: 74,420,684-74,420,737 , GRCh37.p13 chrX: 73,640,519-73,640,572 SLC16A2, LOC105373252
    nsv7092504copy number variation1nstd229human GRCh38 chrX: 74,420,673-74,420,727 , GRCh37.p13 chrX: 73,640,508-73,640,562 SLC16A2, LOC105373252
    nsv7092452copy number variation1nstd229human GRCh38 chrX: 73,923,480-74,457,980 , GRCh37.p13 chrX: 73,143,315-73,677,815 RPS7P14, MIR545, 23 more genes
    nsv7018592inversion1nstd229human GRCh38 chrX: 71,642,458-75,115,067 , GRCh37.p13 chrX: 70,862,308-74,334,902 RN7SL648P, LOC101059915, 83 more genes
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