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Items: 1 to 20 of 154

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5428317copy number variation1nstd206human GRCh38 chr1: 10,462,056-10,462,298 , GRCh37.p13 chr1: 10,522,113-10,522,355 DFFA
    nsv5420361copy number variation1nstd206human GRCh38 chr1: 10,462,132-10,463,900 , GRCh37.p13 chr1: 10,522,189-10,523,957 DFFA
    nsv5370388translocation1nstd200human GRCh38 chr1: 10,457,005-10,457,005 , GRCh38 chr1: 10,457,395-10,457,395 , GRCh37.p13 chr1: 10,517,062-10,517,062 , GRCh37.p13 chr1: 10,517,452-10,517,452 DFFA
    nsv5353873translocation1nstd200human GRCh38 chr1: 10,457,008-10,457,008 , GRCh38 chr13: 50,842,274-50,842,274 , GRCh37.p13 chr1: 10,517,065-10,517,065 , GRCh37.p13 chr13: 51,416,410-51,416,410 DFFA, DLEU7, 1 more genes
    nsv5298736copy number variation1nstd204human GRCh38.p13 chr1: 10,461,131-10,462,047 , GRCh37.p13 chr1: 10,521,188-10,522,104 DFFA
    nsv5074165mobile element insertion1nstd203human GRCh38 chr1: 10,465,977-10,466,005 , GRCh37.p13 chr1: 10,526,034-10,526,062 DFFA
    nsv4889846copy number variation1nstd200human GRCh38 chr1: 10,461,958-10,464,118 , GRCh37.p13 chr1: 10,522,015-10,524,175 DFFA
    nsv4889845copy number variation1nstd200human GRCh38 chr1: 10,461,015-10,468,808 , GRCh37.p13 chr1: 10,521,072-10,528,865 DFFA
    nsv4782934copy number variation1nstd200human GRCh37 chr1: 10,523,102-10,535,879 , GRCh38.p12 chr1: 10,463,045-10,475,822 DFFA, PEX14
    nsv4782933copy number variation1nstd200human GRCh37 chr1: 10,521,980-10,524,162 , GRCh38.p12 chr1: 10,461,923-10,464,105 DFFA
    nsv4782932copy number variation1nstd200human GRCh37 chr1: 10,521,198-10,522,097 , GRCh38.p12 chr1: 10,461,141-10,462,040 DFFA
    nsv4681229copy number variation1nstd102humanUncertain significance GRCh37 chr1: 9,770,494-10,690,064 , GRCh38.p12 chr1: 9,710,436-10,630,007 LOC105376717, MIR5697, 23 more genes
    nsv4674003copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 9,852,396-11,909,475 , GRCh38.p12 chr1: 9,792,338-11,849,418 CLCN6, CORT, 59 more genes
    nsv4517873copy number variation1nstd166human GRCh37.p13 chr1: 10,520,459-10,520,613 , GRCh38.p12 chr1: 10,460,402-10,460,556 DFFA
    nsv4454705copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,246,640-12,841,900 , GRCh38.p12 chr1: 10,186,582-12,781,757 LINC01647, MIR7846, 73 more genes
    nsv4451961copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,524,101-10,640,226 , GRCh38.p12 chr1: 10,464,044-10,580,169 DFFA, PEX14
    nsv4436680complex substitution1nstd102humanUncertain significance GRCh38.p12 chr1: 973,858-24,379,779 , GRCh37 chr1: 909,238-24,706,269 ALPL, RERE, 636 more genes
    nsv4436526complex substitution1nstd102humanUncertain significance GRCh38.p12 chr1: 973,858-16,409,637 , GRCh37 chr1: 909,238-16,736,132 RERE, CA6, 415 more genes
    nsv4436181copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532 LINC01776, IGSF21-AS1, 1853 more genes
    nsv4436105copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-11,784,118 , GRCh38.p12 chr1: 82,154-11,724,061 PARK7, RNF223, 325 more genes
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