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Items: 1 to 20 of 312

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6114973copy number variation1nstd186human GRCh37 chrX: 52,887,783-52,890,056 , GRCh38.p12 chrX: 52,858,754-52,861,027 XAGE3
    nsv6113829mobile element insertion1nstd186human GRCh37 chrX: 52,890,701-52,890,746 , GRCh38.p12 chrX: 52,861,672-52,861,717 XAGE3
    nsv6112721copy number variation1nstd102humanPathogenic GRCh37 chrX: 47,179,068-54,424,785 , GRCh38.p12 chrX: 47,319,669-54,398,352 SNORA11E, SSX11P, 229 more genes
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5974893copy number variation2nstd209human GRCh38 chrX: 52,858,717-52,862,504 , GRCh37.p13 chrX|NW_004070877.1: 2,571,832-2,575,619 , GRCh37.p13 chrX: 52,887,746-52,891,533 XAGE3
    nsv5971180copy number variation1nstd209human GRCh38 chrX: 52,862,005-52,876,733 , GRCh37.p13 chrX: 52,891,034-52,905,764 , GRCh37.p13 chrX|NW_004070877.1: 2,575,120-2,589,848 XAGE3
    nsv5971079copy number variation2nstd209human GRCh38 chrX: 52,858,718-52,861,704 , GRCh37.p13 chrX|NW_004070877.1: 2,571,833-2,574,819 , GRCh37.p13 chrX: 52,887,747-52,890,733 XAGE3
    nsv5968813copy number variation2nstd209human GRCh38 chrX: 52,862,105-52,863,504 , GRCh37.p13 chrX|NW_004070877.1: 2,575,220-2,576,619 , GRCh37.p13 chrX: 52,891,134-52,892,533 XAGE3
    nsv5882057copy number variation1nstd209human GRCh38 chrX: 52,862,950-55,652,570 , GRCh37.p13 chrX: 52,891,979-54,424,077 , GRCh37.p13 chrX|NW_004070877.1: 2,576,065-4,110,759 , MIRLET7F2, 64 more genes
    nsv5869933copy number variation1nstd209human GRCh38 chrX: 52,858,759-52,861,013 , GRCh37.p13 chrX|NW_004070877.1: 2,571,874-2,574,128 , GRCh37.p13 chrX: 52,887,788-52,890,042 XAGE3
    nsv5724797mobile element insertion2nstd211human GRCh38 chrX: 52,861,666-52,861,666 , GRCh37.p13 chrX: 52,890,695-52,890,695 , GRCh37.p13 chrX|NW_004070877.1: 2,574,781-2,574,781 XAGE3
    nsv5668248copy number variation1nstd207human GRCh38 chrX: 52,860,394-52,861,399 , GRCh37.p13 chrX|NW_004070877.1: 2,573,509-2,574,514 , GRCh37.p13 chrX: 52,889,423-52,890,428 XAGE3
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5554599mobile element insertion1nstd206human GRCh38 chrX: 52,861,672-52,861,717 , GRCh37.p13 chrX|NW_004070877.1: 2,574,787-2,574,832 , GRCh37.p13 chrX: 52,890,701-52,890,746 XAGE3
    nsv5422660copy number variation1nstd206human GRCh38 chrX: 52,729,096-52,920,707 , GRCh37.p13 chrX|NW_004070877.1: 2,442,211-2,633,822 , GRCh37.p13 chrX: 52,786,323-52,949,897 XAGE3, XAGE5, 7 more genes
    nsv5420629copy number variation1nstd206human GRCh38 chrX: 52,858,754-52,861,027 , GRCh37.p13 chrX|NW_004070877.1: 2,571,869-2,574,142 , GRCh37.p13 chrX: 52,887,783-52,890,056 XAGE3
    nsv5416491copy number variation1nstd206human GRCh38 chrX: 39,941,083-72,578,519 , GRCh37.p13 chrX: 39,800,337-71,530,833 , USP51, 564 more genes
    nsv5376229translocation1nstd200human GRCh38 chrX: 55,652,520-55,652,520 , GRCh38 chrX: 52,862,974-52,862,974 , GRCh37.p13 chrX|NW_004070877.1: 2,576,089-2,576,089 , GRCh37.p13 chrX: 55,678,953-55,678,953 , GRCh37.p13 chrX: 52,892,003-52,892,003 XAGE3
    nsv5376228translocation1nstd200human GRCh38 chrX: 52,858,755-52,858,755 , GRCh38 chrX: 52,861,022-52,861,022 , GRCh37.p13 chrX: 52,887,784-52,887,784 , GRCh37.p13 chrX|NW_004070877.1: 2,571,870-2,571,870 , GRCh37.p13 chrX: 52,890,051-52,890,051 , GRCh37.p13 chrX|NW_004070877.1: 2,574,137-2,574,137 XAGE3
    nsv5332768translocation1nstd200human GRCh37 chrX: 52,890,052-52,890,052 , GRCh37 chrX: 52,887,783-52,887,783 , GRCh38.p12 chrX: 52,858,754-52,858,754 , GRCh38.p12 chrX: 52,861,023-52,861,023 XAGE3
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