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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3879053copy number variation1nstd102humanLikely pathogenic GRCh37.p13 chrX|NW_003871103.3: 2,965,657-2,990,152 , GRCh38 chrX: 155,531,678-155,556,173 , GRCh37.p13 chrX: 154,761,339-154,785,834 TMLHE
    nsv3872025copy number variation1nstd102humanLikely pathogenic GRCh37.p13 chrX|NW_003871103.3: 2,964,082-2,984,474 , GRCh38 chrX: 155,530,103-155,550,495 , GRCh37.p13 chrX: 154,759,764-154,780,156 TMLHE
    nsv3886529copy number variation1nstd102humanBenign GRCh37 chrX: 154,781,651-154,835,342 , GRCh38.p12 chrX: 155,551,990-155,605,681 TMLHE
    nsv3875269copy number variation1nstd102humanLikely benign GRCh37 chrX: 154,752,980-154,789,496 , GRCh38.p12 chrX: 155,523,319-155,559,835 TMLHE
    nsv3889159copy number variation1nstd102humanBenign GRCh37 chrX: 154,773,360-154,797,420 , GRCh38.p12 chrX: 155,543,699-155,567,759 TMLHE
    nsv3878343copy number variation1nstd102humanBenign GRCh37 chrX: 154,773,360-154,794,657 , GRCh38.p12 chrX: 155,543,699-155,564,996 TMLHE
    nsv3886332copy number variation1nstd102humanBenign GRCh37 chrX: 154,773,360-154,790,404 , GRCh38.p12 chrX: 155,543,699-155,560,743 TMLHE
    nsv3888259copy number variation1nstd102humanBenign GRCh37 chrX: 154,773,360-154,790,307 , GRCh38.p12 chrX: 155,543,699-155,560,646 TMLHE
    nsv3883377copy number variation1nstd102humanBenign GRCh37 chrX: 154,773,360-154,782,179 , GRCh38.p12 chrX: 155,543,699-155,552,518 TMLHE
    nsv3897686copy number variation1nstd102humanBenign GRCh38 chrX: 155,509,742-155,547,057 , NCBI36 chrX: 154,392,597-154,429,912 , GRCh37 chrX: 154,739,403-154,776,718 TMLHE
    nsv4728683copy number variation1nstd102humanUncertain significance GRCh37 chrX: 154,752,099-154,827,787 , GRCh38.p12 chrX: 155,522,438-155,598,126 TMLHE
    nsv4673963copy number variation1nstd102humanUncertain significance GRCh37 chrX: 154,752,979-154,813,224 , GRCh38.p12 chrX: 155,523,318-155,583,563 TMLHE
    nsv4728373copy number variation1nstd102humanUncertain significance GRCh37 chrX: 154,739,499-154,789,638 , GRCh38.p12 chrX: 155,509,838-155,559,977 TMLHE
    nsv6313790copy number variation1nstd102humanUncertain significance GRCh37 chrX: 154,762,224-154,803,688 , GRCh38.p12 chrX: 155,532,563-155,574,027 TMLHE
    nsv6290528copy number variation1nstd102humanUncertain significance GRCh37 chrX: 154,734,432-154,743,564 , GRCh38 chrX: 155,504,771-155,513,903 TMLHE
    nsv6137799copy number variation1nstd102humanUncertain significance GRCh37 chrX: 154,774,757-154,774,937 , GRCh38.p12 chrX: 155,545,096-155,545,276 TMLHE
    nsv4674127copy number variation1nstd102humanLikely benign GRCh37 chrX: 154,739,600-155,000,584 , GRCh38.p12 chrX: 155,509,939-155,770,922 TMLHE, SPRY3
    nsv3896074copy number variation1nstd102humanLikely benign NCBI36 chrX: 154,473,179-154,601,139 , GRCh37 chrX: 154,819,985-154,947,945 , GRCh38 chrX: 155,590,324-155,718,284 TMLHE, SPRY3
    nsv3884526copy number variation1nstd102humanBenign GRCh37 chrX: 154,736,503-154,842,445 , GRCh38.p12 chrX: 155,506,842-155,612,784 TMLHE, SPRY3
    nsv3906676copy number variation1nstd102humanLikely benign NCBI36 chrX: 154,494,472-154,582,499 , GRCh37.p13 chrX|NW_003871103.3: 3,045,596-3,110,903 , GRCh38 chrX: 155,611,617-155,699,644 TMLHE, SPRY3
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