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Items: 1 to 20 of 802

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137734copy number variation1nstd102humanPathogenic GRCh38 chrX: 68,119,248-68,212,212 , GRCh37.p13 chrX: 67,339,090-67,432,054 OPHN1, AKIRIN1P2
    nsv6113233copy number variation1nstd186human GRCh37 chrX: 67,545,427-67,547,798 , GRCh38.p12 chrX: 68,325,585-68,327,956 OPHN1
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5974452copy number variation1nstd209human GRCh38 chrX: 68,217,882-68,227,304 , GRCh37.p13 chrX: 67,437,724-67,447,146 OPHN1
    nsv5875202copy number variation1nstd209human GRCh38 chrX: 68,217,533-68,225,353 , GRCh37.p13 chrX: 67,437,375-67,445,195 OPHN1
    nsv5870487copy number variation1nstd209human GRCh38 chrX: 68,140,588-68,140,661 , GRCh37.p13 chrX: 67,360,430-67,360,503 OPHN1
    nsv5868819copy number variation1nstd209human GRCh38 chrX: 68,325,581-68,327,825 , GRCh37.p13 chrX: 67,545,423-67,547,667 OPHN1
    nsv5867950copy number variation1nstd209human GRCh38 chrX: 68,321,950-68,322,011 , GRCh37.p13 chrX: 67,541,792-67,541,853 OPHN1
    nsv5729805mobile element insertion1nstd211human GRCh38 chrX: 68,168,065-68,168,065 , GRCh37.p13 chrX: 67,387,907-67,387,907 OPHN1
    nsv5723857mobile element insertion1nstd211human GRCh38 chrX: 68,388,010-68,388,010 , GRCh37.p13 chrX: 67,607,852-67,607,852 OPHN1
    nsv5722189mobile element insertion1nstd211human GRCh38 chrX: 68,082,053-68,082,053 , GRCh37.p13 chrX: 67,301,895-67,301,895 OPHN1
    nsv5715795mobile element insertion1nstd211human GRCh38 chrX: 68,406,824-68,406,824 , GRCh37.p13 chrX: 67,626,666-67,626,666 OPHN1
    nsv5666899copy number variation1nstd207human GRCh38 chrX: 68,325,687-68,325,782 , GRCh37.p13 chrX: 67,545,529-67,545,624 OPHN1
    nsv5664625copy number variation1nstd207human GRCh38 chrX: 68,325,581-68,327,825 , GRCh37.p13 chrX: 67,545,423-67,547,667 OPHN1
    nsv5613015insertion1nstd207human GRCh38 chrX: 68,326,722-68,326,722 , GRCh37.p13 chrX: 67,546,564-67,546,564 OPHN1
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5555556mobile element insertion1nstd206human GRCh38 chrX: 68,168,065-68,168,116 , GRCh37.p13 chrX: 67,387,907-67,387,958 OPHN1
    nsv5555537sequence alteration1nstd206human GRCh38 chrX: 68,388,234-68,388,374 , GRCh37.p13 chrX: 67,608,076-67,608,216 OPHN1
    nsv5554058mobile element insertion1nstd206human GRCh38 chrX: 68,388,010-68,388,060 , GRCh37.p13 chrX: 67,607,852-67,607,902 OPHN1
    nsv5433741copy number variation1nstd206human GRCh38 chrX: 68,151,672-68,151,818 , GRCh37.p13 chrX: 67,371,514-67,371,660 OPHN1
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