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Items: 1 to 20 of 289

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960844insertion1nstd209human GRCh38 chr4: 94,122,800-94,122,800 , GRCh37.p13 chr4: 95,043,951-95,043,951 SMARCAD1-DT
    nsv5900936copy number variation1nstd209human GRCh38 chr4: 94,158,443-94,158,536 , GRCh37.p13 chr4: 95,079,594-95,079,687 SMARCAD1-DT
    nsv5689209mobile element insertion1nstd211human GRCh38 chr4: 94,183,405-94,183,405 , GRCh37.p13 chr4: 95,104,556-95,104,556 SMARCAD1-DT
    nsv5564262complex substitution1nstd102humanPathogenic GRCh37.p13 chr4: 95,096,941-95,175,379 , GRCh38 chr4: 94,175,790-94,254,228 SMARCAD1, HMGB3P15, 1 more genes
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5542553insertion1nstd206human GRCh38 chr4: 94,122,803-94,122,851 , GRCh37.p13 chr4: 95,043,954-95,044,002 SMARCAD1-DT
    nsv5470436copy number variation1nstd206human GRCh38 chr4: 94,127,706-94,176,872 , GRCh37.p13 chr4: 95,048,857-95,098,023 SMARCAD1-DT
    nsv5460197copy number variation1nstd206human GRCh38 chr4: 94,166,967-94,167,960 , GRCh37.p13 chr4: 95,088,118-95,089,111 SMARCAD1-DT
    nsv5346859translocation1nstd200human GRCh38 chr4: 94,179,643-94,179,643 , GRCh38 chr4: 94,180,186-94,180,186 , GRCh37.p13 chr4: 95,101,337-95,101,337 , GRCh37.p13 chr4: 95,100,794-95,100,794 SMARCAD1-DT
    nsv5346858translocation1nstd200human GRCh38 chr4: 94,153,307-94,153,307 , GRCh38 chr4: 94,153,819-94,153,819 , GRCh37.p13 chr4: 95,074,458-95,074,458 , GRCh37.p13 chr4: 95,074,970-95,074,970 SMARCAD1-DT
    nsv5309733copy number variation1nstd204human GRCh38.p13 chr4: 93,771,883-94,365,998 , GRCh37.p13 chr4: 94,693,034-95,287,149 ATOH1, GRID2, 5 more genes
    nsv5239337copy number variation1nstd204human GRCh38.p13 chr4: 94,162,511-94,171,820 , GRCh37.p13 chr4: 95,083,662-95,092,971 SMARCAD1-DT
    nsv5231130copy number variation1nstd204human GRCh38.p13 chr4: 94,177,401-94,178,800 , GRCh37.p13 chr4: 95,098,552-95,099,951 SMARCAD1-DT
    nsv5228097copy number variation1nstd204human GRCh38.p13 chr4: 94,177,001-94,181,900 , GRCh37.p13 chr4: 95,098,152-95,103,051 SMARCAD1-DT
    nsv5226684copy number variation1nstd204human GRCh38.p13 chr4: 94,152,840-94,153,839 , GRCh37.p13 chr4: 95,073,991-95,074,990 SMARCAD1-DT
    nsv5223437copy number variation1nstd204human GRCh38.p13 chr4: 94,121,278-94,122,777 , GRCh37.p13 chr4: 95,042,429-95,043,928 SMARCAD1-DT
    nsv5223343copy number variation1nstd204human GRCh37.p13 chr4: 94,692,752-95,287,151 , GRCh38.p13 chr4: 93,771,601-94,366,000 ATOH1, GRID2, 5 more genes
    nsv5090661mobile element insertion1nstd203human GRCh38 chr4: 94,131,757-94,131,771 , GRCh37.p13 chr4: 95,052,908-95,052,922 SMARCAD1-DT
    nsv5087090mobile element insertion1nstd203human GRCh38 chr4: 94,183,388-94,183,405 , GRCh37.p13 chr4: 95,104,539-95,104,556 SMARCAD1-DT
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