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Items: 1 to 20 of 258

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5975962insertion1nstd209human GRCh38 chr12: 106,237,514-106,237,514 , GRCh37.p13 chr12: 106,631,292-106,631,292 CKAP4
    nsv5705741mobile element insertion1nstd211human GRCh38 chr12: 106,238,013-106,238,013 , GRCh37.p13 chr12: 106,631,791-106,631,791 CKAP4
    nsv5548993insertion1nstd206human GRCh38 chr12: 106,241,361-106,241,386 , GRCh37.p13 chr12: 106,635,139-106,635,164 CKAP4
    nsv5508025copy number variation1nstd206human GRCh38 chr12: 106,245,537-106,245,600 , GRCh37.p13 chr12: 106,639,315-106,639,378 CKAP4
    nsv5504144copy number variation1nstd206human GRCh38 chr12: 106,236,244-106,236,781 , GRCh37.p13 chr12: 106,630,022-106,630,559 CKAP4
    nsv5037136inversion1nstd200human GRCh38 chr12: 69,787,024-109,882,221 , GRCh37.p13 chr12: 70,180,804-110,320,026 , RPL23AP68, 540 more genes
    nsv4995456copy number variation1nstd200human GRCh38 chr12: 106,241,393-106,246,795 , GRCh37.p13 chr12: 106,635,171-106,640,573 CKAP4
    nsv4993641copy number variation1nstd200human GRCh38 chr12: 106,236,244-106,236,781 , GRCh37.p13 chr12: 106,630,022-106,630,559 CKAP4
    nsv4886161inversion1nstd200human GRCh37 chr12: 70,180,810-110,320,027 , GRCh38.p12 chr12: 69,787,030-109,882,222 , LOC728739, 540 more genes
    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
    nsv4728881copy number variation1nstd102humanPathogenic GRCh37 chr12: 106,498,814-112,252,906 , GRCh38.p12 chr12: 106,105,036-111,815,102 ATP2A2, CUX2, 115 more genes
    nsv4675779copy number variation1nstd102humanUncertain significance GRCh37 chr12: 106,510,497-107,070,575 , GRCh38.p12 chr12: 106,116,719-106,676,797 RNU7-94P, POLR3B, 6 more genes
    nsv4670653copy number variation1nstd186human GRCh37 chr12: 106,640,836-106,642,276 , GRCh38.p12 chr12: 106,247,058-106,248,498 CKAP4
    nsv4615101copy number variation1nstd183human GRCh37 chr12: 106,640,868-106,642,266 , GRCh38.p12 chr12: 106,247,090-106,248,488 CKAP4
    nsv4613793copy number variation1nstd183human GRCh37 chr12: 106,641,120-106,641,732 , GRCh38.p12 chr12: 106,247,342-106,247,954 CKAP4
    nsv4611350copy number variation1nstd183human GRCh37 chr12: 106,641,179-106,641,732 , GRCh38.p12 chr12: 106,247,401-106,247,954 CKAP4
    nsv4607538copy number variation1nstd183human GRCh37 chr12: 106,641,270-106,641,732 , GRCh38.p12 chr12: 106,247,492-106,247,954 CKAP4
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