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Items: 1 to 20 of 210

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977816inversion1nstd209human GRCh38 chr12: 120,681,283-120,681,860 , GRCh37.p13 chr12: 121,119,086-121,119,663 CABP1, LOC105370029
    nsv5973346inversion1nstd209human GRCh38 chr12: 118,054,601-123,705,841 , GRCh37.p13 chr12: 118,492,406-124,190,388 , ACADS, 162 more genes
    nsv5709379mobile element insertion1nstd211human GRCh38 chr12: 120,673,212-120,673,212 , GRCh37.p13 chr12: 121,111,015-121,111,015 CABP1
    nsv5647954insertion1nstd207human GRCh38 chr12: 120,657,466-120,657,466 , GRCh37.p13 chr12: 121,095,269-121,095,269 CABP1
    nsv5555463sequence alteration1nstd206human GRCh38 chr12: 120,561,097-121,398,447 , GRCh37.p13 chr12: 120,998,900-121,761,800 P2RX7, OASL, 27 more genes
    nsv5507592copy number variation1nstd206human GRCh38 chr12: 120,661,821-120,662,926 , GRCh37.p13 chr12: 121,099,624-121,100,729 CABP1
    nsv5419963mobile element insertion1nstd206human GRCh38 chr12: 120,673,212-120,673,263 , GRCh37.p13 chr12: 121,111,015-121,111,066 CABP1
    nsv5320210copy number variation1nstd204human GRCh38.p13 chr12: 120,645,183-120,645,955 , GRCh37.p13 chr12: 121,082,986-121,083,758 CABP1
    nsv5316483copy number variation1nstd204human GRCh38.p13 chr12: 120,661,840-120,662,906 , GRCh37.p13 chr12: 121,099,643-121,100,709 CABP1
    nsv4995988copy number variation1nstd200human GRCh38 chr12: 120,661,864-120,662,884 , GRCh37.p13 chr12: 121,099,667-121,100,687 CABP1
    nsv4995987copy number variation1nstd200human GRCh38 chr12: 120,646,628-120,647,443 , GRCh37.p13 chr12: 121,084,431-121,085,246 CABP1
    nsv4993759copy number variation1nstd200human GRCh38 chr12: 120,643,001-120,772,078 , GRCh37.p13 chr12: 121,080,804-121,209,881 CABP1, MLEC, 5 more genes
    nsv4846621copy number variation1nstd200human GRCh37 chr12: 121,080,804-121,209,881 , GRCh38.p12 chr12: 120,643,001-120,772,078 ACADS, MLEC, 5 more genes
    nsv4843232copy number variation1nstd200human GRCh37 chr12: 121,099,667-121,100,687 , GRCh38.p12 chr12: 120,661,864-120,662,884 CABP1
    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
    nsv4576604mobile element insertion1nstd166human GRCh37.p13 chr12: 121,082,522-121,082,522 , GRCh38.p12 chr12: 120,644,719-120,644,719 CABP1
    nsv4563671sequence alteration1nstd166human GRCh37.p13 chr12: 120,998,865-121,836,049 , GRCh38.p12 chr12: 120,561,062-121,398,246 ACADS, P2RX4, 27 more genes
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