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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6315540copy number variation1nstd102humanPathogenic GRCh37 chr9: 129,376,720-129,463,802 , GRCh38.p12 chr9: 126,614,441-126,701,523 LMX1B
    nsv6313248copy number variation1nstd102humanPathogenic GRCh37 chr9: 129,376,729-129,458,730 , GRCh38.p12 chr9: 126,614,450-126,696,451 LMX1B
    nsv4349485copy number variation1nstd102humanPathogenic GRCh37 chr9: 129,414,011-129,460,757 , GRCh38.p12 chr9: 126,651,732-126,698,478 LMX1B
    nsv6312748copy number variation1nstd102humanPathogenic GRCh37 chr9: 129,453,095-129,458,730 , GRCh38.p12 chr9: 126,690,816-126,696,451 LMX1B
    nsv7097685copy number variation1nstd102humanPathogenic GRCh37 chr9: 129,376,729-129,377,868 , GRCh38.p12 chr9: 126,614,450-126,615,589 LMX1B
    nsv5673880copy number variation1nstd102humanPathogenic GRCh37 chr9: 129,376,729-129,377,858 , GRCh38.p12 chr9: 126,614,450-126,615,579 LMX1B
    nsv7098052copy number variation1nstd102humanPathogenic GRCh37 chr9: 129,377,642-129,377,868 , GRCh38.p12 chr9: 126,615,363-126,615,589 LMX1B
    nsv997158copy number variation1nstd45humanPathogenic GRCh38.p12 chr9: 126,614,443-126,701,032 , GRCh37 chr9: 129,376,722-129,463,311 LMX1B
    nsv7097686copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 129,453,095-129,453,367 , GRCh38.p12 chr9: 126,690,816-126,691,088 LMX1B
    nsv3901042copy number variation1nstd102humanBenign GRCh37 chr9: 129,407,543-129,422,451 , GRCh38.p12 chr9: 126,645,264-126,660,172 LMX1B
    nsv3916575copy number variation1nstd102humanBenign NCBI36 chr9: 128,490,284-128,495,411 , GRCh38 chr9: 126,688,184-126,693,311 , GRCh37 chr9: 129,450,463-129,455,590 LMX1B
    nsv3918493copy number variation1nstd102humanUncertain significance NCBI36 chr9: 128,499,457-128,507,948 , GRCh37 chr9: 129,459,636-129,468,127 , GRCh38 chr9: 126,697,357-126,705,848 LMX1B
    nsv3904124copy number variation1nstd102humanBenign GRCh37 chr9: 129,370,440-129,513,586 , GRCh38.p12 chr9: 126,608,161-126,751,307 LMX1B, LMX1B-DT, 1 more genes
    nsv4676021copy number variation1nstd102humanUncertain significance GRCh37 chr9: 129,137,576-129,384,914 , GRCh38.p12 chr9: 126,375,297-126,622,635 LMX1B, LMX1B-DT, 3 more genes
    nsv3896498copy number variation1nstd102humanUncertain significance GRCh37 chr9: 129,416,212-129,644,627 , GRCh38.p12 chr9: 126,653,933-126,882,348 LMX1B, LOC107987129, 2 more genes
    nsv4457037copy number variation1nstd102humanUncertain significance GRCh37 chr9: 129,251,840-129,409,117 , GRCh38.p12 chr9: 126,489,561-126,646,838 LMX1B, MVB12B, 2 more genes
    nsv6637870copy number variation1nstd102humanUncertain significance GRCh37 chr9: 129,256,988-129,403,346 , GRCh38.p12 chr9: 126,494,709-126,641,067 LMX1B, LMX1B-DT, 2 more genes
    nsv4729056copy number variation1nstd102humanUncertain significance GRCh37 chr9: 129,257,643-129,403,346 , GRCh38.p12 chr9: 126,495,364-126,641,067 LMX1B, MVB12B, 2 more genes
    nsv3919744copy number variation1nstd102humanUncertain significance GRCh38 chr9: 126,517,522-126,646,975 , GRCh37 chr9: 129,279,801-129,409,254 , NCBI36 chr9: 128,319,622-128,449,075 LMX1B, LMX1B-DT, 1 more genes
    nsv6634298copy number variation1nstd102humanPathogenic GRCh38 chr9: 126,507,040-126,804,072 , GRCh37.p13 chr9: 129,269,319-129,566,351 LMX1B, ZBTB43, 4 more genes
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