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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5910429copy number variation1nstd209human GRCh38 chr12: 34,050,005-38,345,840 , GRCh37.p13 chr12: 34,202,940-38,739,642 LOC107984469, ALG10B, 12 more genes
    nsv5849519copy number variation1nstd209human GRCh38 chr12: 38,319,537-38,321,272 , GRCh37.p13 chr12: 38,713,339-38,715,074 ALG10B
    nsv5663886insertion1nstd207human GRCh38 chr12: 38,317,557-38,317,557 , GRCh37.p13 chr12: 38,711,359-38,711,359 ALG10B
    nsv5593719copy number variation1nstd207human GRCh38 chr12: 38,329,734-38,331,318 , GRCh37.p13 chr12: 38,723,536-38,725,120 ALG10B
    nsv5564512copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 37,873,948-49,578,619 , GRCh38.p12 chr12: 37,480,146-49,184,836 ADCY6, ABCD2, 187 more genes
    nsv5503313copy number variation1nstd206human GRCh38 chr12: 37,972,128-38,480,128 , GRCh37.p13 chr12: 38,365,930-38,873,930 TUBB8P5, ALG10B, 7 more genes
    nsv5502576copy number variation1nstd206human GRCh38 chr12: 38,320,170-38,326,037 , GRCh37.p13 chr12: 38,713,972-38,719,839 ALG10B
    nsv5499975copy number variation1nstd206human GRCh38 chr12: 38,316,789-38,318,563 , GRCh37.p13 chr12: 38,710,591-38,712,365 ALG10B
    nsv5280372copy number variation1nstd204human GRCh38.p13 chr12: 38,319,187-38,326,056 , GRCh37.p13 chr12: 38,712,989-38,719,858 ALG10B
    nsv5280359copy number variation1nstd204human GRCh38.p13 chr12: 38,315,735-38,318,140 , GRCh37.p13 chr12: 38,709,537-38,711,942 ALG10B
    nsv5029954inversion1nstd200human GRCh38 chr12: 38,328,571-48,487,625 , GRCh37.p13 chr12: 38,722,373-48,881,408 , MESDP1, 138 more genes
    nsv4985493copy number variation1nstd200human GRCh38 chr12: 38,102,302-38,463,416 , GRCh37.p13 chr12: 38,496,104-38,857,218 RNA5SP359, ALG10B, 5 more genes
    nsv4985418copy number variation1nstd200human GRCh38 chr12: 37,810,196-38,520,707 , GRCh37.p13 chr12: 38,203,998-38,914,509 NF1P12, LOC100421618, 7 more genes
    nsv4985356copy number variation1nstd200human GRCh38 chr12: 37,715,920-38,330,509 , GRCh37.p13 chr12: 38,109,722-38,724,311 TUBB8P5, AK6P2, 7 more genes
    nsv4842686copy number variation1nstd200human GRCh37 chr12: 38,496,104-38,857,218 , GRCh38.p12 chr12: 38,102,302-38,463,416 RNA5SP359, TUBB8P5, 5 more genes
    nsv4835167copy number variation1nstd200human GRCh37 chr12: 38,109,722-38,724,311 , GRCh38.p12 chr12: 37,715,920-38,330,509 RNA5SP359, LOC107984469, 7 more genes
    nsv4833204copy number variation1nstd200human GRCh37 chr12: 38,203,998-38,914,509 , GRCh38.p12 chr12: 37,810,196-38,520,707 ALG10B, AK6P2, 7 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4609231copy number variation1nstd183human GRCh37 chr12: 38,568,939-38,751,754 , GRCh38.p12 chr12: 38,175,137-38,357,952 TUBB8P5, ALG10B, 2 more genes
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