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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv5980446copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718 LINC02641, CFAP46, 194 more genes
    nsv5980347insertion1nstd209human GRCh38 chr10: 124,639,122-124,639,122 , GRCh37.p13 chr10: 126,327,691-126,327,691 FAM53B
    nsv5717544mobile element insertion1nstd211human GRCh38 chr10: 124,633,225-124,633,225 , GRCh37.p13 chr10: 126,321,794-126,321,794 FAM53B
    nsv5378351translocation1nstd200human GRCh38 chr6: 31,047,116-31,047,116 , GRCh38 chr10: 124,633,240-124,633,240 , GRCh37.p13 chr6: 31,014,893-31,014,893 , GRCh37.p13 chr10: 126,321,809-126,321,809 FAM53B
    nsv5373317translocation1nstd200human GRCh38 chr10: 124,715,877-124,715,877 , GRCh38 chr10: 124,712,997-124,712,997 , GRCh37.p13 chr10: 126,401,566-126,401,566 , GRCh37.p13 chr10: 126,404,446-126,404,446 FAM53B-AS1, FAM53B
    nsv5354560translocation1nstd200human GRCh38 chr10: 124,697,452-124,697,452 , GRCh38 chr10: 124,695,288-124,695,288 , GRCh37.p13 chr10: 126,386,021-126,386,021 , GRCh37.p13 chr10: 126,383,857-126,383,857 FAM53B
    nsv5354559translocation1nstd200human GRCh38 chr10: 124,619,985-124,619,985 , GRCh38 chr22: 31,020,294-31,020,294 , GRCh37.p13 chr10: 126,308,554-126,308,554 , GRCh37.p13 chr22: 31,416,280-31,416,280 , FAM53B
    nsv5330998translocation1nstd200human GRCh37 chr10: 126,383,857-126,383,857 , GRCh37 chr10: 126,386,021-126,386,021 , GRCh38.p12 chr10: 124,695,288-124,695,288 , GRCh38.p12 chr10: 124,697,452-124,697,452 FAM53B
    nsv4983963copy number variation1nstd200human GRCh38 chr10: 124,537,451-124,639,711 , GRCh37.p13 chr10: 126,226,020-126,328,280 , FAM53B, 1 more genes
    nsv4977386copy number variation1nstd200human GRCh38 chr10: 124,720,219-124,720,327 , GRCh37.p13 chr10: 126,408,788-126,408,896 FAM53B
    nsv4977385copy number variation1nstd200human GRCh38 chr10: 124,712,969-124,714,208 , GRCh37.p13 chr10: 126,401,538-126,402,777 FAM53B-AS1, FAM53B
    nsv4977384copy number variation1nstd200human GRCh38 chr10: 124,683,224-124,684,371 , GRCh37.p13 chr10: 126,371,793-126,372,940 FAM53B
    nsv4977383copy number variation1nstd200human GRCh38 chr10: 124,659,432-124,666,201 , GRCh37.p13 chr10: 126,348,001-126,354,770 FAM53B
    nsv4977382copy number variation1nstd200human GRCh38 chr10: 124,627,782-124,634,292 , GRCh37.p13 chr10: 126,316,351-126,322,861 FAM53B
    nsv4849199copy number variation1nstd200human GRCh37 chr10: 126,371,793-126,372,940 , GRCh38.p12 chr10: 124,683,224-124,684,371 FAM53B
    nsv4846101copy number variation1nstd200human GRCh37 chr10: 126,402,231-126,403,210 , GRCh38.p12 chr10: 124,713,662-124,714,641 FAM53B-AS1, FAM53B
    nsv4845022copy number variation1nstd200human GRCh37 chr10: 126,316,351-126,322,861 , GRCh38.p12 chr10: 124,627,782-124,634,292 FAM53B
    nsv4836931copy number variation1nstd200human GRCh37 chr10: 126,226,020-126,328,280 , GRCh38.p12 chr10: 124,537,451-124,639,711 , FAM53B, 1 more genes
    nsv4835942copy number variation1nstd200human GRCh37 chr10: 126,348,001-126,354,770 , GRCh38.p12 chr10: 124,659,432-124,666,201 FAM53B
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