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Items: 1 to 20 of 214

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6121857copy number variation1nstd186human GRCh37 chr15: 67,534,479-67,534,799 , GRCh38.p12 chr15: 67,242,141-67,242,461 AAGAB
    nsv5939660copy number variation1nstd209human GRCh38 chr15: 67,246,785-67,246,849 , GRCh37.p13 chr15: 67,539,123-67,539,187 AAGAB
    nsv5937428copy number variation1nstd209human GRCh38 chr15: 67,242,127-67,242,460 , GRCh37.p13 chr15: 67,534,465-67,534,798 AAGAB
    nsv5933942copy number variation1nstd209human GRCh38 chr15: 67,216,159-67,220,839 , GRCh37.p13 chr15: 67,508,497-67,513,177 AAGAB
    nsv5853779copy number variation1nstd209human GRCh38 chr15: 67,217,548-67,221,608 , GRCh37.p13 chr15: 67,509,886-67,513,946 AAGAB
    nsv5705574mobile element insertion2nstd211human GRCh38 chr15: 67,208,167-67,208,167 , GRCh37.p13 chr15: 67,500,505-67,500,505 AAGAB
    nsv5672747copy number variation1nstd102humanPathogenic GRCh37 chr15: 67,546,897-67,571,850 , GRCh38.p12 chr15: 67,254,559-67,279,512 IQCH, AAGAB
    nsv5650660insertion1nstd207human GRCh38 chr15: 67,208,153-67,208,153 , GRCh37.p13 chr15: 67,500,491-67,500,491 AAGAB
    nsv5594040copy number variation1nstd207human GRCh38 chr15: 67,242,127-67,242,460 , GRCh37.p13 chr15: 67,534,465-67,534,798 AAGAB
    nsv5593426copy number variation1nstd207human GRCh38 chr15: 67,246,628-67,246,693 , GRCh37.p13 chr15: 67,538,966-67,539,031 AAGAB
    nsv5539976insertion1nstd206human GRCh38 chr15: 67,208,153-67,208,153 , GRCh37.p13 chr15: 67,500,491-67,500,491 AAGAB
    nsv5520488copy number variation1nstd206human GRCh38 chr15: 67,242,141-67,242,461 , GRCh37.p13 chr15: 67,534,479-67,534,799 AAGAB
    nsv5382432mobile element deletion2nstd186human GRCh37 chr15: 67,534,479-67,534,799 , GRCh38.p12 chr15: 67,242,141-67,242,461 AAGAB
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5349092translocation1nstd200human GRCh38 chr15: 67,249,746-67,249,746 , GRCh38 chr15: 67,249,655-67,249,655 , GRCh37.p13 chr15: 67,541,993-67,541,993 , GRCh37.p13 chr15: 67,542,084-67,542,084 AAGAB
    nsv5279586copy number variation1nstd204human GRCh38.p13 chr15: 67,213,975-67,216,674 , GRCh37.p13 chr15: 67,506,313-67,509,012 AAGAB
    nsv5213860mobile element deletion1nstd204human GRCh38.p13 chr15: 67,242,141-67,242,461 , GRCh37.p13 chr15: 67,534,479-67,534,799 AAGAB
    nsv5149138mobile element insertion1nstd203human GRCh38 chr15: 67,208,153-67,208,167 , GRCh37.p13 chr15: 67,500,491-67,500,505 AAGAB
    nsv4992119copy number variation1nstd200human GRCh38 chr15: 67,254,038-67,254,104 , GRCh37.p13 chr15: 67,546,376-67,546,442 IQCH, AAGAB
    nsv4992118copy number variation1nstd200human GRCh38 chr15: 67,244,280-67,246,443 , GRCh37.p13 chr15: 67,536,618-67,538,781 AAGAB
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