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Items: 1 to 20 of 345

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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
    nsv6714025copy number variation1nstd229human GRCh38 chr3: 45,654,958-45,658,588 , GRCh37.p13 chr3: 45,696,450-45,700,080 LIMD1
    nsv6708118copy number variation1nstd229human GRCh38 chr3: 45,594,820-45,594,845 , GRCh37.p13 chr3: 45,636,312-45,636,337 LIMD1
    nsv6704961copy number variation1nstd229human GRCh38 chr3: 45,589,905-45,592,807 , GRCh37.p13 chr3: 45,631,397-45,634,299 LIMD1
    nsv6704609copy number variation1nstd229human GRCh38 chr3: 45,593,616-45,594,370 , GRCh37.p13 chr3: 45,635,108-45,635,862 LIMD1
    nsv6701030copy number variation1nstd229human GRCh38 chr3: 45,673,101-45,682,700 , GRCh37.p13 chr3: 45,714,593-45,724,192 LIMD1, LIMD1-AS1
    nsv6698548copy number variation1nstd229human GRCh38 chr3: 45,512,806-45,614,439 , GRCh37.p13 chr3: 45,554,298-45,655,931 LARS2, LIMD1
    nsv6636411copy number variation1nstd102humanUncertain significance GRCh37 chr3: 45,648,926-45,699,671 , GRCh38.p12 chr3: 45,607,434-45,658,179 LIMD1
    nsv6553910inversion1nstd223human GRCh38 chr3: 45,654,598-45,655,209 , GRCh37.p13 chr3: 45,696,090-45,696,701 LIMD1
    nsv6552525inversion1nstd223human GRCh38 chr3: 45,645,967-45,646,597 , GRCh37.p13 chr3: 45,687,459-45,688,089 LIMD1
    nsv6374614copy number variation1nstd223human GRCh38 chr3: 45,664,216-45,665,346 , GRCh37.p13 chr3: 45,705,708-45,706,838 LIMD1
    nsv6371510copy number variation1nstd223human GRCh38 chr3: 45,678,121-45,685,315 , GRCh37.p13 chr3: 45,719,613-45,726,807 LIMD1, LIMD1-AS1
    nsv6368131copy number variation1nstd223human GRCh38 chr3: 45,631,326-45,632,872 , GRCh37.p13 chr3: 45,672,818-45,674,364 LIMD1
    nsv6365579copy number variation1nstd223human GRCh38 chr3: 45,506,627-45,604,642 , GRCh37.p13 chr3: 45,548,119-45,646,134 LARS2, LIMD1, 1 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
    nsv6263363copy number variation1nstd214human GRCh38 chr3: 45,675,543-45,675,614 , GRCh37.p13 chr3: 45,717,035-45,717,106 LIMD1
    nsv6253954mobile element insertion1nstd215human GRCh38 chr3: 45,651,015-45,651,015 , GRCh37.p13 chr3: 45,692,507-45,692,507 LIMD1
    nsv6253953mobile element insertion1nstd215human GRCh38 chr3: 45,649,862-45,649,862 , GRCh37.p13 chr3: 45,691,354-45,691,354 LIMD1
    nsv6253952mobile element insertion1nstd215human GRCh38 chr3: 45,638,027-45,638,027 , GRCh37.p13 chr3: 45,679,519-45,679,519 LIMD1
    nsv6134813copy number variation1nstd213human GRCh37 chr3: 44,650,000-45,860,001 , GRCh38.p12 chr3: 44,608,508-45,818,509 TGM4, CLEC3B, 35 more genes
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