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Items: 1 to 20 of 162

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4681321copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chrX: 37,639,262-37,670,190 , GRCh38.p12 chrX: 37,780,009-37,810,937 CYBB
    nsv6314655copy number variation1nstd102humanPathogenic GRCh37 chrX: 37,639,331-37,670,170 , GRCh38.p12 chrX: 37,780,078-37,810,917 CYBB
    nsv7098522copy number variation1nstd102humanPathogenic GRCh37 chrX: 37,639,262-37,660,621 , GRCh38.p12 chrX: 37,780,009-37,801,368 CYBB
    nsv7098657copy number variation1nstd102humanPathogenic GRCh37 chrX: 37,658,188-37,670,170 , GRCh38.p12 chrX: 37,798,935-37,810,917 CYBB
    nsv4452336copy number variation1nstd102humanPathogenic GRCh37 chrX: 37,639,262-37,642,873 , GRCh38 chrX: 37,780,009-37,783,620 CYBB
    nsv4682493copy number variation1nstd102humanPathogenic GRCh37 chrX: 37,639,262-37,641,456 , GRCh38.p12 chrX: 37,780,009-37,782,203 CYBB
    nsv997132copy number variation1nstd45humanPathogenic GRCh37 chrX: 37,639,270-37,672,714 , GRCh38.p12 chrX: 37,780,017-37,813,461 CYBB
    nsv4683567copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 37,670,024-37,670,190 , GRCh38.p12 chrX: 37,810,771-37,810,937 CYBB
    nsv6313219copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 37,641,330-37,641,446 , GRCh38.p12 chrX: 37,782,077-37,782,193 CYBB
    nsv6314654copy number variation1nstd102humanUncertain significance GRCh37 chrX: 37,639,269-37,672,715 , GRCh38.p12 chrX: 37,780,016-37,813,462 CYBB
    nsv7098521copy number variation1nstd102humanPathogenic GRCh37 chrX: 37,545,215-37,670,170 , GRCh38.p12 chrX: 37,685,962-37,810,917 CYBB, XK
    nsv7098410copy number variation1nstd102humanPathogenic GRCh37 chrX: 37,545,215-37,664,441 , GRCh38.p12 chrX: 37,685,962-37,805,188 CYBB, XK
    nsv6315263copy number variation1nstd102humanPathogenic GRCh37 chrX: 37,550,041-37,645,092 , GRCh38.p12 chrX: 37,690,788-37,785,839 CYBB, XK
    nsv3893297copy number variation1nstd102humanBenign GRCh38 chrX: 37,564,515-37,871,920 , NCBI36 chrX: 37,308,687-37,616,117 , GRCh37.p13 chrX|NW_003871099.1: 276,321-522,319 CYBB, DYNLT3, 3 more genes
    nsv3904162copy number variation1nstd102humanPathogenic GRCh38 chrX: 10,001-156,030,895 , GRCh37 chrX: 60,001-155,260,560 , NCBI36 chrX: 1-154,913,754 CYBB, NANOGNBP3, 2154 more genes
    nsv3913255copy number variation2nstd102humanPathogenic NCBI36 chrX: 701-154,913,754 , GRCh37.p13 chrX: 60,701-155,260,560 , GRCh38.p12 chrX: 10,701-156,030,895 CYBB, NHS-AS1, 2154 more genes
    nsv3907094copy number variation4nstd102humanPathogenic GRCh38 chrX: 10,679-156,022,206 , GRCh37 chrX: 60,679-155,251,871 , NCBI36 chrX: 679-154,905,065 CYBB, GPR119, 2153 more genes
    nsv3878553copy number variation2nstd102humanPathogenic GRCh37 chrX: 60,262-155,245,765 , GRCh38.p12 chrX: 10,262-156,016,100 CYBB, H2AB2, 2152 more genes
    nsv3898149copy number variation1nstd102humanPathogenic GRCh38 chrX: 20,297-156,026,127 , NCBI36 chrX: 10,297-154,908,986 , GRCh37 chrX: 70,297-155,255,792 CYBB, OR3B1P, 2154 more genes
    nsv3877395copy number variation1nstd102humanPathogenic GRCh37 chrX: 71,267-155,255,839 , GRCh38.p12 chrX: 21,267-156,026,174 CYBB, ARMCX2, 2154 more genes
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