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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5700259mobile element insertion1nstd211human GRCh38 chr12: 52,804,884-52,804,884 , GRCh37.p13 chr12: 53,198,668-53,198,668 KRT3, KRT4
    nsv5427440mobile element insertion1nstd206human GRCh38 chr12: 52,804,884-52,804,935 , GRCh37.p13 chr12: 53,198,668-53,198,719 KRT4, KRT3
    nsv5130436mobile element insertion1nstd203human GRCh38 chr12: 52,805,771-52,805,788 , GRCh37.p13 chr12: 53,199,555-53,199,572 KRT3, KRT4
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 ARL2BPP2, SNORA70G, 686 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 MYO1A, SPRYD3, 769 more genes
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 R3HDM2, RXYLT1, 769 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 ACACB, ACADS, 1787 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 RNA5SP368, LINC02555, 1787 more genes
    nsv4675782copy number variation1nstd102humanUncertain significance GRCh37 chr12: 52,914,323-53,238,344 , GRCh38.p12 chr12: 52,520,539-52,844,560 LOC105369772, KRT4, 20 more genes
    nsv4559196inversion1nstd166human GRCh37.p13 chr12: 51,569,865-55,219,228 , GRCh38.p12 chr12: 51,176,082-54,825,444 AMHR2, ATP5MC2, 163 more genes
    nsv4545757insertion1nstd166human GRCh37.p13 chr12: 53,203,932-53,203,932 , GRCh38.p12 chr12: 52,810,148-52,810,148 KRT4
    nsv4324772inversion1nstd166human GRCh37.p13 chr12: 27,368,635-91,765,744 , GRCh38.p12 chr12: 27,215,702-91,371,967 ADCY6, ABCD2, 1101 more genes
    nsv4192991copy number variation1nstd166human GRCh37.p13 chr12: 53,199,355-53,199,963 , GRCh38.p12 chr12: 52,805,571-52,806,179 KRT3, KRT4
    nsv3929131insertion1nstd167human GRCh37 chr12: 53,207,583-53,207,583 , GRCh38.p12 chr12: 52,813,799-52,813,799 KRT4
    nsv3924549copy number variation1nstd102humanPathogenic GRCh38 chr12: 50,633,888-52,851,909 , NCBI36 chr12: 49,313,938-51,531,960 , GRCh37 chr12: 51,027,671-53,245,693 KRT80, KRT83, 86 more genes
    nsv3922322copy number variation1nstd102humanLikely benign GRCh38 chr12: 52,748,391-52,950,618 , NCBI36 chr12: 51,428,442-51,630,669 , GRCh37 chr12: 53,142,175-53,344,402 BTBD10P1, KRT3, 10 more genes
    nsv3920847inversion1nstd102humanUncertain significance GRCh38.p12 chr12: 26,217,318-53,967,754 , GRCh37 chr12: 26,370,251-54,361,538 ASIC1, ACVR1B, 503 more genes
    nsv3914194copy number variation1nstd102humanPathogenic NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807 RNF34, LOC107984468, 2523 more genes
    nsv3912656copy number variation1nstd102humanPathogenic NCBI36 chr12: 48,802,409-51,928,511 , GRCh37 chr12: 50,516,142-53,642,244 , GRCh38 chr12: 50,122,359-53,248,460 KRT83, RPL26P33, 116 more genes
    nsv3905447copy number variation2nstd102humanPathogenic GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316 NTS, LINC02388, 2524 more genes
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