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Items: 1 to 20 of 268

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148122copy number variation1nstd102humanUncertain significance GRCh37 chr12: 106,460,580-107,090,224 , GRCh38.p12 chr12: 106,066,802-106,696,446 POLR3B, TCP11L2, 7 more genes
    nsv7075931inversion1nstd229human GRCh38 chr12: 106,237,689-106,398,315 , GRCh37.p13 chr12: 106,631,467-106,792,093 RNU7-94P, POLR3B, 2 more genes
    nsv6926568copy number variation1nstd229human GRCh38 chr12: 106,243,288-106,243,652 , GRCh37.p13 chr12: 106,637,066-106,637,430 CKAP4
    nsv6471669copy number variation1nstd223human GRCh38 chr12: 106,236,244-106,236,779 , GRCh37.p13 chr12: 106,630,022-106,630,557 CKAP4
    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
    nsv6248558mobile element insertion1nstd215human GRCh38 chr12: 106,238,013-106,238,013 , GRCh37.p13 chr12: 106,631,791-106,631,791 CKAP4
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132211copy number variation1nstd213human GRCh37 chr12: 106,280,000-106,630,001 , GRCh38.p12 chr12: 105,886,222-106,236,223 NUAK1, CKAP4, 2 more genes
    nsv6132136copy number variation1nstd213human GRCh37 chr12: 105,300,000-106,660,001 , GRCh38.p12 chr12: 104,906,222-106,266,223 NUAK1, CKAP4, 20 more genes
    nsv6132135copy number variation1nstd213human GRCh37 chr12: 105,280,000-106,660,001 , GRCh38.p12 chr12: 104,886,222-106,266,223 NUAK1, CKAP4, 20 more genes
    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
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