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Items: 1 to 20 of 359

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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
    nsv5867917copy number variation1nstd209human GRCh38 chrX: 80,330,024-80,330,076 , GRCh37.p13 chrX: 79,585,523-79,585,575 CHMP1B2P
    nsv5729606mobile element insertion1nstd211human GRCh38 chrX: 80,295,053-80,295,053 , GRCh37.p13 chrX: 79,550,552-79,550,552 CHMP1B2P
    nsv5726289mobile element insertion1nstd211human GRCh38 chrX: 80,229,567-80,229,567 , GRCh37.p13 chrX: 79,485,066-79,485,066 CHMP1B2P
    nsv5718397mobile element insertion2nstd211human GRCh38 chrX: 80,315,762-80,315,762 , GRCh37.p13 chrX: 79,571,261-79,571,261 CHMP1B2P
    nsv5622456insertion1nstd207human GRCh38 chrX: 80,325,765-80,325,765 , GRCh37.p13 chrX: 79,581,264-79,581,264 CHMP1B2P
    nsv5620309insertion1nstd207human GRCh38 chrX: 80,325,566-80,325,566 , GRCh37.p13 chrX: 79,581,065-79,581,065 CHMP1B2P
    nsv5620084insertion1nstd207human GRCh38 chrX: 80,315,754-80,315,754 , GRCh37.p13 chrX: 79,571,253-79,571,253 CHMP1B2P
    nsv5611170insertion1nstd207human GRCh38 chrX: 80,325,619-80,325,619 , GRCh37.p13 chrX: 79,581,118-79,581,118 CHMP1B2P
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5558966mobile element insertion1nstd206human GRCh38 chrX: 80,315,762-80,315,813 , GRCh37.p13 chrX: 79,571,261-79,571,312 CHMP1B2P
    nsv5555605mobile element insertion1nstd206human GRCh38 chrX: 80,229,567-80,229,618 , GRCh37.p13 chrX: 79,485,066-79,485,117 CHMP1B2P
    nsv5426662copy number variation1nstd206human GRCh38 chrX: 80,225,110-80,228,279 , GRCh37.p13 chrX: 79,480,609-79,483,778 CHMP1B2P
    nsv5376565translocation1nstd200human GRCh38 chrX: 80,277,161-80,277,161 , GRCh38 chrX: 80,277,049-80,277,049 , GRCh37.p13 chrX: 79,532,548-79,532,548 , GRCh37.p13 chrX: 79,532,660-79,532,660 CHMP1B2P
    nsv5197817mobile element insertion1nstd203human GRCh38 chrX: 80,315,754-80,315,762 , GRCh37.p13 chrX: 79,571,253-79,571,261 CHMP1B2P
    nsv5197675mobile element insertion1nstd203human GRCh38 chrX: 80,315,753-80,315,767 , GRCh37.p13 chrX: 79,571,252-79,571,266 CHMP1B2P
    nsv5059979copy number variation1nstd102humanPathogenic GRCh37 chrX: 56,469,080-155,233,731 , GRCh38.p12 chrX: 56,442,647-156,004,066 VDAC1P1, LOC105373299, 1364 more genes
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 more genes
    nsv4908479copy number variation1nstd200human GRCh38 chrX: 80,321,738-80,324,334 , GRCh37.p13 chrX: 79,577,237-79,579,833 CHMP1B2P
    nsv4908478copy number variation1nstd200human GRCh38 chrX: 80,316,490-80,318,284 , GRCh37.p13 chrX: 79,571,989-79,573,783 CHMP1B2P
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