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Items: 1 to 20 of 118

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6937724copy number variation1nstd229human GRCh38 chr12: 110,460,501-110,470,600 , GRCh37.p13 chr12: 110,898,306-110,908,405 RPL31P49, FAM216A, 1 more genes
    nsv6931732copy number variation1nstd229human GRCh38 chr12: 108,914,683-113,697,537 , GRCh37.p13 chr12: 109,308,459-114,135,342 PTPN11, RPL31P49, 111 more genes
    nsv6927238copy number variation1nstd229human GRCh38 chr12: 110,441,811-110,460,615 , GRCh37.p13 chr12: 110,879,616-110,898,420 GPN3, ARPC3, 1 more genes
    nsv6589693inversion1nstd223human GRCh38 chr12: 110,455,220-110,456,101 , GRCh37.p13 chr12: 110,893,025-110,893,906 GPN3
    nsv6291583copy number variation1nstd102humanPathogenic GRCh37 chr12: 104,230,462-111,984,801 , GRCh38.p12 chr12: 103,836,684-111,546,997 LOC105369964, LOC644746, 147 more genes
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132137copy number variation1nstd213human GRCh37 chr12: 110,580,000-111,480,001 , GRCh38.p12 chr12: 110,142,195-111,042,197 CUX2, IFT81, 21 more genes
    nsv5975897insertion1nstd209human GRCh38 chr12: 110,450,831-110,450,831 , GRCh37.p13 chr12: 110,888,636-110,888,636 ARPC3, GPN3
    nsv5939699copy number variation1nstd209human GRCh38 chr12: 110,462,814-110,476,251 , GRCh37.p13 chr12: 110,900,619-110,914,056 FAM216A, GPN3
    nsv5862824copy number variation1nstd209human GRCh38 chr12: 110,464,649-110,472,048 , GRCh37.p13 chr12: 110,902,454-110,909,853 GPN3, FAM216A
    nsv5859370copy number variation2nstd209human GRCh38 chr12: 110,456,628-110,458,027 , GRCh37.p13 chr12: 110,894,433-110,895,832 GPN3
    nsv5273674copy number variation1nstd204human GRCh37.p13 chr12: 110,813,506-110,955,705 , GRCh38.p13 chr12: 110,375,701-110,517,900 ARPC3, FAM216A, 6 more genes
    nsv4995580copy number variation1nstd200human GRCh38 chr12: 110,463,281-110,463,401 , GRCh37.p13 chr12: 110,901,086-110,901,206 GPN3
    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
    nsv4603063copy number variation1nstd183human GRCh37 chr12: 110,891,911-110,893,813 , GRCh38.p12 chr12: 110,454,106-110,456,008 GPN3
    nsv4219153copy number variation1nstd166human GRCh37.p13 chr12: 110,899,369-110,900,647 , GRCh38.p12 chr12: 110,461,564-110,462,842 RPL31P49, GPN3
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