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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
    nsv5970935copy number variation1nstd209human GRCh38 chrX: 65,623,017-65,624,416 , GRCh37.p13 chrX: 64,842,896-64,844,295 MSN
    nsv5878955copy number variation1nstd209human GRCh38 chrX: 65,623,043-65,624,624 , GRCh37.p13 chrX: 64,842,922-64,844,503 MSN
    nsv5730876mobile element insertion1nstd211human GRCh38 chrX: 65,670,941-65,670,941 , GRCh37.p13 chrX: 64,890,802-64,890,802 MSN
    nsv5721904mobile element insertion2nstd211human GRCh38 chrX: 65,681,815-65,681,815 , GRCh37.p13 chrX: 64,901,676-64,901,676 MSN
    nsv5623624insertion1nstd207human GRCh38 chrX: 65,665,167-65,665,167 , GRCh37.p13 chrX: 64,885,034-64,885,034 MSN
    nsv5610636insertion1nstd207human GRCh38 chrX: 65,681,801-65,681,801 , GRCh37.p13 chrX: 64,901,662-64,901,662 MSN
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5559329mobile element insertion1nstd206human GRCh38 chrX: 65,681,815-65,681,866 , GRCh37.p13 chrX: 64,901,676-64,901,727 MSN
    nsv5542194insertion1nstd206human GRCh38 chrX: 65,621,076-65,621,076 , GRCh37.p13 chrX: 64,840,955-64,840,955 MSN
    nsv5427233copy number variation1nstd206human GRCh38 chrX: 65,685,501-65,702,389 , GRCh37.p13 chrX: 64,905,362-64,922,251 MSN
    nsv5425679copy number variation1nstd206human GRCh38 chrX: 65,592,748-65,676,026 , GRCh37.p13 chrX: 64,812,628-64,895,887 , MSN
    nsv5421837copy number variation1nstd206human GRCh38 chrX: 65,675,503-65,675,563 , GRCh37.p13 chrX: 64,895,364-64,895,424 MSN
    nsv5419342copy number variation1nstd206human GRCh38 chrX: 65,635,822-65,655,847 , GRCh37.p13 chrX: 64,855,701-64,875,714 MSN
    nsv5416491copy number variation1nstd206human GRCh38 chrX: 39,941,083-72,578,519 , GRCh37.p13 chrX: 39,800,337-71,530,833 , USP51, 564 more genes
    nsv5415815copy number variation1nstd206human GRCh38 chrX: 65,623,043-65,624,625 , GRCh37.p13 chrX: 64,842,922-64,844,504 MSN
    nsv5376383translocation1nstd200human GRCh38 chrX: 65,658,401-65,658,401 , GRCh38 chrX: 65,658,474-65,658,474 , GRCh37.p13 chrX: 64,878,341-64,878,341 , GRCh37.p13 chrX: 64,878,268-64,878,268 MSN
    nsv5376382translocation1nstd200human GRCh38 chrX: 65,628,071-65,628,071 , GRCh38 chrX: 65,660,642-65,660,642 , GRCh37.p13 chrX: 64,847,950-64,847,950 , GRCh37.p13 chrX: 64,880,509-64,880,509 MSN
    nsv5376381translocation1nstd200human GRCh38 chrX: 65,637,193-65,637,193 , GRCh38 chrX: 65,626,656-65,626,656 , GRCh37.p13 chrX: 64,846,535-64,846,535 , GRCh37.p13 chrX: 64,857,072-64,857,072 MSN
    nsv5376380translocation1nstd200human GRCh38 chrX: 65,609,102-65,609,102 , GRCh38 chrX: 65,593,062-65,593,062 , GRCh37.p13 chrX: 64,812,942-64,812,942 , GRCh37.p13 chrX: 64,828,982-64,828,982 MSN
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