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Items: 1 to 20 of 291

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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
    nsv5886927copy number variation1nstd209human GRCh38 chrX: 73,813,713-73,813,847 , GRCh37.p13 chrX: 73,033,548-73,033,682 TSIX
    nsv5880738copy number variation1nstd209human GRCh38 chrX: 69,751,799-78,490,154 , GRCh37.p13 chrX: 68,971,643-77,745,651 , MTND4P31, 183 more genes
    nsv5871663copy number variation1nstd209human GRCh38 chrX: 73,802,942-73,803,012 , GRCh37.p13 chrX: 73,022,777-73,022,847 TSIX
    nsv5666670copy number variation1nstd207human GRCh38 chrX: 73,802,942-73,803,012 , GRCh37.p13 chrX: 73,022,777-73,022,847 TSIX
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5428842copy number variation1nstd206human GRCh38 chrX: 73,813,761-73,815,055 , GRCh37.p13 chrX: 73,033,596-73,034,890 TSIX
    nsv5427810copy number variation1nstd206human GRCh38 chrX: 73,786,749-74,066,861 , GRCh37.p13 chrX: 73,006,584-73,286,696 RPSAP14, XIST, 5 more genes
    nsv5422084copy number variation1nstd206human GRCh38 chrX: 73,802,942-73,803,013 , GRCh37.p13 chrX: 73,022,777-73,022,848 TSIX
    nsv5416387copy number variation1nstd206human GRCh38 chrX: 73,813,707-73,813,851 , GRCh37.p13 chrX: 73,033,542-73,033,686 TSIX
    nsv5180535mobile element insertion1nstd203human GRCh38 chrX: 73,814,894-73,814,910 , GRCh37.p13 chrX: 73,034,729-73,034,745 TSIX
    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
    nsv4908426copy number variation1nstd200human GRCh38 chrX: 73,815,966-73,817,699 , GRCh37.p13 chrX: 73,035,801-73,037,534 TSIX
    nsv4905616copy number variation1nstd200human GRCh38 chrX: 73,669,580-73,905,018 , GRCh37.p13 chrX: 72,889,415-73,124,853 XIST, SEPHS1P4, 3 more genes
    nsv4782104copy number variation1nstd200human GRCh37 chrX: 72,889,415-73,124,853 , GRCh38.p12 chrX: 73,669,580-73,905,018 CHIC1, XIST, 3 more genes
    nsv4771473copy number variation1nstd200human GRCh37 chrX: 73,035,801-73,037,532 , GRCh38.p12 chrX: 73,815,966-73,817,697 TSIX
    nsv4771472copy number variation1nstd200human GRCh37 chrX: 73,033,596-73,034,890 , GRCh38.p12 chrX: 73,813,761-73,815,055 TSIX
    nsv4769249copy number variation1nstd201human GRCh37 chrX: 61,728,816-155,233,846 , GRCh38.p12 chrX: 62,509,346-156,004,181 , ABCB7, 1364 more genes
    nsv4728499copy number variation1nstd102humanPathogenic GRCh37 chrX: 55,507,789-155,198,481 , GRCh38.p12 chrX: 55,481,356-155,968,816 GABRE, RN7SL325P, 1371 more genes
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