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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
    nsv7083970copy number variation1nstd229human GRCh38 chrX: 132,949,240-132,996,534 , GRCh37.p13 chrX: 132,083,268-132,130,562 HS6ST2
    nsv7083969copy number variation1nstd229human GRCh38 chrX: 132,947,004-132,960,722 , GRCh37.p13 chrX: 132,081,032-132,094,750 HS6ST2
    nsv7083968copy number variation1nstd229human GRCh38 chrX: 132,904,832-132,907,524 , GRCh37.p13 chrX: 132,038,860-132,041,552 HS6ST2, NAA20P1
    nsv7083967copy number variation1nstd229human GRCh38 chrX: 132,902,301-132,911,838 , GRCh37.p13 chrX: 132,036,329-132,045,866 HS6ST2, NAA20P1
    nsv7083966copy number variation1nstd229human GRCh38 chrX: 132,893,632-132,904,773 , GRCh37.p13 chrX: 132,027,660-132,038,801 HS6ST2
    nsv7083965copy number variation1nstd229human GRCh38 chrX: 132,869,301-132,872,700 , GRCh37.p13 chrX: 132,003,329-132,006,728 HS6ST2
    nsv7083964copy number variation1nstd229human GRCh38 chrX: 132,868,804-132,879,381 , GRCh37.p13 chrX: 132,002,832-132,013,409 HS6ST2
    nsv7083963copy number variation1nstd229human GRCh38 chrX: 132,868,313-132,878,837 , GRCh37.p13 chrX: 132,002,341-132,012,865 HS6ST2
    nsv7083962copy number variation1nstd229human GRCh38 chrX: 132,868,301-132,878,800 , GRCh37.p13 chrX: 132,002,329-132,012,828 HS6ST2
    nsv7083961copy number variation1nstd229human GRCh38 chrX: 132,865,601-132,871,900 , GRCh37.p13 chrX: 131,999,629-132,005,928 HS6ST2
    nsv7083960copy number variation1nstd229human GRCh38 chrX: 132,865,501-132,871,900 , GRCh37.p13 chrX: 131,999,529-132,005,928 HS6ST2
    nsv7083959copy number variation1nstd229human GRCh38 chrX: 132,855,201-133,021,400 , GRCh37.p13 chrX: 131,989,229-132,155,428 HS6ST2, NAA20P1
    nsv7083958copy number variation1nstd229human GRCh38 chrX: 132,849,524-132,855,373 , GRCh37.p13 chrX: 131,983,552-131,989,401 HS6ST2
    nsv7083957copy number variation1nstd229human GRCh38 chrX: 132,810,368-132,814,100 , GRCh37.p13 chrX: 131,944,396-131,948,128 HS6ST2
    nsv7083956copy number variation1nstd229human GRCh38 chrX: 132,806,939-132,814,079 , GRCh37.p13 chrX: 131,940,967-131,948,107 HS6ST2
    nsv7083955copy number variation1nstd229human GRCh38 chrX: 132,806,419-132,806,979 , GRCh37.p13 chrX: 131,940,447-131,941,007 HS6ST2
    nsv7083954copy number variation1nstd229human GRCh38 chrX: 132,806,395-132,806,917 , GRCh37.p13 chrX: 131,940,423-131,940,945 HS6ST2
    nsv7083953copy number variation1nstd229human GRCh38 chrX: 132,806,394-132,806,836 , GRCh37.p13 chrX: 131,940,422-131,940,864 HS6ST2
    nsv7083952copy number variation1nstd229human GRCh38 chrX: 132,805,406-132,807,518 , GRCh37.p13 chrX: 131,939,434-131,941,546 HS6ST2
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