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Items: 1 to 20 of 677

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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
    nsv5970979copy number variation1nstd209human GRCh38 chrX: 2,714,915-2,774,110 , GRCh37.p13 chrX: 2,632,956-2,692,151 CD99, XG
    nsv5968112copy number variation1nstd209human GRCh38 chrX: 2,706,131-2,720,361 , GRCh37.p13 chrX: 2,624,172-2,638,402 CD99
    nsv5954337insertion1nstd209human GRCh38 chrX: 2,724,037-2,724,037 , GRCh37.p13 chrX: 2,642,078-2,642,078 CD99
    nsv5882480copy number variation1nstd209human GRCh38 chrX: 2,690,644-2,690,836 , GRCh37.p13 chrX: 2,608,685-2,608,877 CD99
    nsv5719739mobile element insertion1nstd211human GRCh38 chrX: 2,714,305-2,714,305 , GRCh37.p13 chrX: 2,632,346-2,632,346 CD99
    nsv5671782inversion1nstd207human GRCh38 chrY: 10,002-57,217,414 , GRCh37.p13 chrY: 10,002-59,363,565 , ACTG1P2, 580 more genes
    nsv5670661copy number variation1nstd207human GRCh38 chrX: 2,690,644-2,690,836 , GRCh37.p13 chrX: 2,608,685-2,608,877 CD99
    nsv5669584copy number variation1nstd207human GRCh38 chrX: 2,732,357-2,732,806 , GRCh37.p13 chrX: 2,650,398-2,650,847 CD99
    nsv5667177copy number variation1nstd207human GRCh38 chrY: 2,690,658-2,690,850 , GRCh37.p13 chrY: 2,558,699-2,558,891 CD99
    nsv5621860insertion1nstd207human GRCh38 chrY: 2,724,037-2,724,037 , GRCh37.p13 chrY: 2,592,078-2,592,078 CD99
    nsv5611762insertion1nstd207human GRCh38 chrX: 2,724,037-2,724,037 , GRCh37.p13 chrX: 2,642,078-2,642,078 CD99
    nsv5605490insertion1nstd207human GRCh38 chrX: 2,732,721-2,732,721 , GRCh37.p13 chrX: 2,650,762-2,650,762 CD99
    nsv5605381insertion1nstd207human GRCh38 chrY: 2,732,721-2,732,721 , GRCh37.p13 chrY: 2,600,762-2,600,762 CD99
    nsv5564472copy number variation1nstd102humanPathogenic GRCh37 chrY: 10,701-5,080,415 , GRCh38.p12 chrY: 10,701-5,212,374 AGPAT5P1, NAP1L1P2, 58 more genes
    nsv5553918mobile element insertion1nstd206human GRCh38 chrX: 2,714,305-2,714,356 , GRCh37.p13 chrX: 2,632,346-2,632,397 CD99
    nsv5541313insertion1nstd206human GRCh38 chrX: 2,724,037-2,724,037 , GRCh37.p13 chrX: 2,642,078-2,642,078 CD99
    nsv5432327copy number variation1nstd206human GRCh38 chrX: 10,000-2,781,000 , GRCh37.p13 chrX: 60,001-2,699,041 , IL3RA, 40 more genes
    nsv5431814copy number variation1nstd206human GRCh38 chrX: 2,531,036-2,924,507 , GRCh37.p13 chrX: 2,449,077-2,842,548 ARSD, CD99, 7 more genes
    nsv5425986copy number variation1nstd206human GRCh38 chrX: 2,704,735-2,706,007 , GRCh37.p13 chrX: 2,622,776-2,624,048 CD99
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