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Items: 1 to 20 of 369

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6113195copy number variation1nstd186human GRCh37 chrX: 72,819,011-72,831,723 , GRCh38.p12 chrX: 73,599,175-73,611,888 CHIC1
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5979757copy number variation1nstd209human GRCh38 chrX: 73,627,493-73,636,692 , GRCh37.p13 chrX: 72,847,328-72,856,527 CHIC1
    nsv5971789copy number variation1nstd209human GRCh38 chrX: 73,599,173-73,610,226 , GRCh37.p13 chrX: 72,819,009-72,830,062 CHIC1
    nsv5966754insertion1nstd209human GRCh38 chrX: 73,594,784-73,594,784 , GRCh37.p13 chrX: 72,814,620-72,814,620 CHIC1
    nsv5885249copy number variation1nstd209human GRCh38 chrX: 73,628,695-73,636,645 , GRCh37.p13 chrX: 72,848,530-72,856,480 CHIC1
    nsv5881326copy number variation1nstd209human GRCh38 chrX: 73,633,717-73,633,801 , GRCh37.p13 chrX: 72,853,552-72,853,636 CHIC1
    nsv5880738copy number variation1nstd209human GRCh38 chrX: 69,751,799-78,490,154 , GRCh37.p13 chrX: 68,971,643-77,745,651 , MTND4P31, 183 more genes
    nsv5879659copy number variation1nstd209human GRCh38 chrX: 73,655,462-73,655,523 , GRCh37.p13 chrX: 72,875,297-72,875,358 CHIC1
    nsv5727763mobile element insertion1nstd211human GRCh38 chrX: 73,592,313-73,592,313 , GRCh37.p13 chrX: 72,812,149-72,812,149 CHIC1
    nsv5716121mobile element insertion1nstd211human GRCh38 chrX: 73,602,320-73,602,320 , GRCh37.p13 chrX: 72,822,156-72,822,156 CHIC1
    nsv5670283copy number variation1nstd207human GRCh38 chrX: 73,599,200-73,611,887 , GRCh37.p13 chrX: 72,819,036-72,831,722 CHIC1
    nsv5666420copy number variation1nstd207human GRCh38 chrX: 73,655,483-73,655,546 , GRCh37.p13 chrX: 72,875,318-72,875,381 CHIC1
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5557162mobile element insertion1nstd206human GRCh38 chrX: 73,592,313-73,592,364 , GRCh37.p13 chrX: 72,812,149-72,812,200 CHIC1
    nsv5426889copy number variation1nstd206human GRCh38 chrX: 73,599,175-73,611,888 , GRCh37.p13 chrX: 72,819,011-72,831,723 CHIC1
    nsv5422356copy number variation1nstd206human GRCh38 chrX: 73,628,700-73,636,646 , GRCh37.p13 chrX: 72,848,535-72,856,481 CHIC1
    nsv5415840copy number variation1nstd206human GRCh38 chrX: 73,672,890-73,672,988 , GRCh37.p13 chrX: 72,892,725-72,892,823 CHIC1
    nsv5376483translocation1nstd200human GRCh38 chrX: 73,659,394-73,659,394 , GRCh38 chrX: 73,659,340-73,659,340 , GRCh37.p13 chrX: 72,879,175-72,879,175 , GRCh37.p13 chrX: 72,879,229-72,879,229 CHIC1
    nsv5376482translocation1nstd200human GRCh38 chrX: 73,636,646-73,636,646 , GRCh38 chrX: 73,628,700-73,628,700 , GRCh37.p13 chrX: 72,856,481-72,856,481 , GRCh37.p13 chrX: 72,848,535-72,848,535 CHIC1
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