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Items: 1 to 20 of 701

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5973645copy number variation1nstd209human GRCh38 chrX: 1,391,092-1,400,080 , GRCh37.p13 chrX: 1,509,985-1,518,973 , SLC25A6, 2 more genes
    nsv5971507copy number variation2nstd209human GRCh38 chrX: 1,399,481-1,400,929 , GRCh37.p13 chrX: 1,518,374-1,519,822 LINC00106, ASMTL-AS1
    nsv5871512copy number variation1nstd209human GRCh38 chrX: 1,395,659-1,396,162 , GRCh37.p13 chrX: 1,514,552-1,515,055 , LINC00106
    nsv5671782inversion1nstd207human GRCh38 chrY: 10,002-57,217,414 , GRCh37.p13 chrY: 10,002-59,363,565 , ACTG1P2, 580 more genes
    nsv5564472copy number variation1nstd102humanPathogenic GRCh37 chrY: 10,701-5,080,415 , GRCh38.p12 chrY: 10,701-5,212,374 AGPAT5P1, NAP1L1P2, 58 more genes
    nsv5556906sequence alteration1nstd206human GRCh38 chrX: 1,348,093-1,930,225 , GRCh37.p13 chrX: 1,466,986-2,049,118 , ASMTL-AS1, 14 more genes
    nsv5432327copy number variation1nstd206human GRCh38 chrX: 10,000-2,781,000 , GRCh37.p13 chrX: 60,001-2,699,041 , IL3RA, 40 more genes
    nsv5430141copy number variation1nstd206human GRCh38 chrX: 1,398,682-1,406,067 , GRCh37.p13 chrX: 1,517,575-1,524,960 ASMTL-AS1, LINC00106, 1 more genes
    nsv5418515copy number variation1nstd206human GRCh38 chrX: 864,608-1,428,971 , GRCh37.p13 chrX: 932,710-1,547,864 , SLC25A6, 15 more genes
    nsv5415997copy number variation1nstd206human GRCh38 chrX: 1,392,930-1,481,303 , GRCh37.p13 chrX: 1,511,823-1,600,196 , ASMTL-AS1, 3 more genes
    nsv5366323translocation1nstd200human GRCh38 chrX: 1,406,067-1,406,067 , GRCh38 chrX: 1,398,682-1,398,682 , GRCh37.p13 chrX: 1,517,575-1,517,575 , GRCh37.p13 chrX: 1,524,960-1,524,960 ASMTL, ASMTL-AS1, 1 more genes
    nsv5338839translocation1nstd200human GRCh37 chrX: 1,514,616-1,514,616 , GRCh37 chrX: 1,515,047-1,515,047 , GRCh38.p12 chrX: 1,395,723-1,395,723 , GRCh38.p12 chrX: 1,396,154-1,396,154 , LINC00106
    nsv5059968copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-56,457,794 , GRCh38.p12 chrX: 251,879-56,431,361 PAGE3, METTL15P3, 785 more genes
    nsv4905060copy number variation1nstd200human GRCh38 chrX: 1,210,273-1,496,953 , GRCh37.p13 chrX: 1,329,166-1,615,846 , LINC00106, 13 more genes
    nsv4905055copy number variation1nstd200human GRCh38 chrX: 1,162,318-1,452,888 , GRCh37.p13 chrX: 1,262,471-1,571,781 , MIR3690, 13 more genes
    nsv4778826copy number variation1nstd200human GRCh37 chrX: 1,517,575-1,524,960 , GRCh38.p12 chrX: 1,398,682-1,406,067 LINC00106, ASMTL-AS1, 1 more genes
    nsv4778821copy number variation1nstd200human GRCh37 chrX: 1,461,821-1,580,170 , GRCh38.p12 chrX: 1,342,928-1,461,277 , SLC25A6, 6 more genes
    nsv4778816copy number variation1nstd200human GRCh37 chrX: 1,404,936-1,810,906 , GRCh38.p12 chrX: 1,286,043-1,692,013 , MIR3690, 14 more genes
    nsv4772432copy number variation1nstd200human GRCh37 chrX: 1,397,219-1,698,248 , GRCh38.p12 chrX: 1,278,326-1,579,355 , LINC00106, 11 more genes
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