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Items: 1 to 20 of 183

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6123039copy number variation1nstd186human GRCh37 chr12: 124,430,520-124,430,572 , GRCh38.p12 chr12: 123,945,973-123,946,025 CCDC92
    nsv6121931copy number variation1nstd186human GRCh37 chr12: 124,457,728-124,458,430 , GRCh38.p12 chr12: 123,973,181-123,973,883 CCDC92, ZNF664, 1 more genes
    nsv5967933inversion1nstd209human GRCh38 chr12: 123,965,476-123,965,852 , GRCh37.p13 chr12: 124,450,023-124,450,399 CCDC92
    nsv5935538copy number variation1nstd209human GRCh38 chr12: 123,973,301-123,973,882 , GRCh37.p13 chr12: 124,457,848-124,458,429 CCDC92, ZNF664, 1 more genes
    nsv5653094insertion2nstd207human GRCh38 chr12: 123,945,973-123,945,973 , GRCh37.p13 chr12: 124,430,520-124,430,520 CCDC92
    nsv5554579inversion1nstd206human GRCh38 chr12: 123,965,482-123,965,869 , GRCh37.p13 chr12: 124,450,029-124,450,416 CCDC92
    nsv5507803copy number variation1nstd206human GRCh38 chr12: 123,973,181-123,973,883 , GRCh37.p13 chr12: 124,457,728-124,458,430 CCDC92, ZNF664-RFLNA, 1 more genes
    nsv5504058copy number variation1nstd206human GRCh38 chr12: 123,945,973-123,946,025 , GRCh37.p13 chr12: 124,430,520-124,430,572 CCDC92
    nsv5381782copy number variation1nstd102humanPathogenic GRCh37 chr12: 123,878,845-126,829,341 , GRCh38.p12 chr12: 123,394,298-126,344,795 DDX55, ZNF664, 55 more genes
    nsv5374563translocation1nstd200human GRCh38 chr12: 123,973,109-123,973,109 , GRCh38 chr2: 3,884,045-3,884,045 , GRCh37.p13 chr12: 124,457,656-124,457,656 , GRCh37.p13 chr2: 3,931,635-3,931,635 CCDC92, ZNF664, 1 more genes
    nsv5303513copy number variation1nstd204human GRCh38.p13 chr12: 123,956,137-123,956,722 , GRCh37.p13 chr12: 124,440,684-124,441,269 CCDC92
    nsv4996202copy number variation1nstd200human GRCh38 chr12: 123,964,773-123,966,182 , GRCh37.p13 chr12: 124,449,320-124,450,729 CCDC92
    nsv4880111inversion1nstd200human GRCh37 chr12: 124,450,029-124,450,400 , GRCh38.p12 chr12: 123,965,482-123,965,853 CCDC92
    nsv4834386copy number variation1nstd200human GRCh37 chr12: 124,440,688-124,441,260 , GRCh38.p12 chr12: 123,956,141-123,956,713 CCDC92
    nsv4829936copy number variation1nstd200human GRCh37 chr12: 124,449,320-124,450,729 , GRCh38.p12 chr12: 123,964,773-123,966,182 CCDC92
    nsv4756222insertion1nstd199human GRCh37 chr12: 124,430,534-124,430,534 , GRCh38.p12 chr12: 123,945,987-123,945,987 CCDC92
    nsv4756208inversion1nstd199human GRCh37 chr12: 104,359,633-125,801,147 , GRCh38.p12 chr12: 103,965,855-125,316,601 , ACACB, 453 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4754840inversion1nstd199human GRCh37 chr12: 104,382,539-125,801,164 , GRCh38.p12 chr12: 103,988,761-125,316,618 , ACACB, 452 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
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