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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
    nsv5976160inversion1nstd209human GRCh38 chrX: 68,979,629-71,845,571 , GRCh37.p13 chrX: 68,199,472-71,065,421 ARR3, DLG3, 73 more genes
    nsv5884909copy number variation1nstd209human GRCh38 chrX: 71,399,612-71,399,937 , GRCh37.p13 chrX: 70,619,462-70,619,787 TAF1
    nsv5880738copy number variation1nstd209human GRCh38 chrX: 69,751,799-78,490,154 , GRCh37.p13 chrX: 68,971,643-77,745,651 , MTND4P31, 183 more genes
    nsv5876601copy number variation1nstd209human GRCh38 chrX: 71,451,122-71,451,431 , GRCh37.p13 chrX: 70,670,972-70,671,281 TAF1
    nsv5727158mobile element insertion1nstd211human GRCh38 chrX: 71,491,068-71,491,068 , GRCh37.p13 chrX: 70,710,918-70,710,918 TAF1, INGX
    nsv5718996mobile element insertion1nstd211human GRCh38 chrX: 71,467,106-71,467,106 , GRCh37.p13 chrX: 70,686,956-70,686,956 TAF1
    nsv5670097copy number variation1nstd207human GRCh38 chrX: 71,520,430-71,522,095 , GRCh37.p13 chrX: 70,740,280-70,741,945 TAF1
    nsv5668866copy number variation1nstd207human GRCh38 chrX: 71,520,430-71,521,262 , GRCh37.p13 chrX: 70,740,280-70,741,112 TAF1
    nsv5668796copy number variation1nstd207human GRCh38 chrX: 71,452,079-71,452,131 , GRCh37.p13 chrX: 70,671,929-70,671,981 TAF1
    nsv5667027copy number variation1nstd207human GRCh38 chrX: 71,523,282-71,523,814 , GRCh37.p13 chrX: 70,743,132-70,743,664 TAF1
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5426554copy number variation1nstd206human GRCh38 chrX: 71,519,648-71,525,545 , GRCh37.p13 chrX: 70,739,498-70,745,395 TAF1
    nsv5422083copy number variation1nstd206human GRCh38 chrX: 71,429,208-71,430,412 , GRCh37.p13 chrX: 70,649,058-70,650,262 TAF1
    nsv5420972copy number variation1nstd206human GRCh38 chrX: 71,452,268-71,452,363 , GRCh37.p13 chrX: 70,672,118-70,672,213 TAF1
    nsv5416491copy number variation1nstd206human GRCh38 chrX: 39,941,083-72,578,519 , GRCh37.p13 chrX: 39,800,337-71,530,833 , USP51, 564 more genes
    nsv5376454translocation1nstd200human GRCh38 chrX: 71,451,124-71,451,124 , GRCh38 chrX: 71,451,432-71,451,432 , GRCh37.p13 chrX: 70,670,974-70,670,974 , GRCh37.p13 chrX: 70,671,282-70,671,282 TAF1
    nsv5376452translocation1nstd200human GRCh38 chrX: 71,455,998-71,455,998 , GRCh38 chrX: 71,342,498-71,342,498 , GRCh37.p13 chrX: 70,562,348-70,562,348 , GRCh37.p13 chrX: 70,675,848-70,675,848 TAF1
    nsv5343327translocation1nstd200human GRCh37 chrX: 70,685,057-70,685,057 , GRCh37 chrX: 24,690,367-24,690,367 , GRCh38.p12 chrX: 24,672,250-24,672,250 , GRCh38.p12 chrX: 71,465,207-71,465,207 PCYT1B, TAF1
    nsv5198222mobile element insertion1nstd203human GRCh38 chrX: 71,490,526-71,490,526 , GRCh37.p13 chrX: 70,710,376-70,710,376 TAF1, INGX
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