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Items: 1 to 20 of 187

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096805copy number variation1nstd102humanUncertain significance GRCh37 chr3: 45,435,946-49,137,751 , GRCh38.p12 chr3: 45,394,454-49,100,318 SNORA94, LIMD1-AS1, 120 more genes
    nsv6717725copy number variation1nstd229human GRCh38 chr3: 48,584,801-48,598,600 , GRCh37.p13 chr3: 48,622,234-48,636,033 COL7A1, UQCRC1
    nsv6711244copy number variation1nstd229human GRCh38 chr3: 48,593,201-48,635,400 , GRCh37.p13 chr3: 48,630,634-48,672,833 TMEM89, COL7A1, 5 more genes
    nsv6708120copy number variation1nstd229human GRCh38 chr3: 48,552,177-48,594,105 , GRCh37.p13 chr3: 48,589,610-48,631,538 MIR711, UCN2, 2 more genes
    nsv6706853copy number variation1nstd229human GRCh38 chr3: 48,574,501-48,576,000 , GRCh37.p13 chr3: 48,611,934-48,613,433 COL7A1
    nsv6702008copy number variation1nstd229human GRCh38 chr3: 48,590,530-48,593,651 , GRCh37.p13 chr3: 48,627,963-48,631,084 COL7A1
    nsv6700836copy number variation1nstd229human GRCh38 chr3: 48,056,801-51,204,000 , GRCh37.p13 chr3: 48,098,291-51,241,431 APEH, SLC26A6, 129 more genes
    nsv6372055copy number variation1nstd223human GRCh38 chr3: 48,386,801-49,230,000 , GRCh37.p13 chr3: 48,428,291-49,267,433 NCKIPSD, UCN2, 44 more genes
    nsv6365306copy number variation1nstd223human GRCh38 chr3: 48,429,601-48,926,800 , GRCh37.p13 chr3: 48,471,010-48,964,233 PRKAR2A-AS1, SNORA94, 25 more genes
    nsv6315166copy number variation1nstd102humanPathogenic GRCh37 chr3: 44,948,482-49,115,809 , GRCh38.p12 chr3: 44,906,990-49,078,376 TMEM89, TGM4, 129 more genes
    nsv6134694copy number variation1nstd213human GRCh37 chr3: 46,170,000-52,140,001 , GRCh38.p12 chr3: 46,128,508-52,105,985 ACY1, AMT, 210 more genes
    nsv5993492copy number variation1nstd212human GRCh38 chr3: 48,566,011-48,566,101 , GRCh37.p13 chr3: 48,603,444-48,603,534 COL7A1
    nsv5902529copy number variation1nstd209human GRCh38 chr3: 48,582,554-48,582,640 , GRCh37.p13 chr3: 48,619,987-48,620,073 COL7A1
    nsv5673730copy number variation1nstd102humanPathogenic GRCh37 chr3: 48,602,206-48,617,500 , GRCh38.p12 chr3: 48,564,773-48,580,067 MIR711, COL7A1
    nsv5673729copy number variation1nstd102humanPathogenic GRCh37 chr3: 48,507,870-50,340,407 , GRCh38.p12 chr3: 48,466,471-50,302,976 SEMA3B-AS1, GNAT1, 87 more genes
    nsv5673564copy number variation1nstd102humanPathogenic GRCh37 chr3: 48,601,829-48,632,780 , GRCh38.p12 chr3: 48,564,396-48,595,347 MIR711, COL7A1
    nsv5613400insertion1nstd207human GRCh38 chr3: 48,585,603-48,585,603 , GRCh37.p13 chr3: 48,623,036-48,623,036 COL7A1
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5452504copy number variation1nstd206human GRCh38 chr3: 48,566,013-48,566,101 , GRCh37.p13 chr3: 48,603,446-48,603,534 COL7A1
    nsv5438088copy number variation1nstd206human GRCh38 chr3: 48,582,554-48,582,641 , GRCh37.p13 chr3: 48,619,987-48,620,074 COL7A1
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