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Items: 1 to 20 of 106

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5938912copy number variation1nstd209human GRCh38 chr12: 104,301,376-104,302,527 , GRCh37.p13 chr12: 104,695,154-104,696,305 EID3, TXNRD1
    nsv5499549copy number variation1nstd206human GRCh38 chr12: 104,156,533-104,412,768 , GRCh37.p13 chr12: 104,550,311-104,806,546 RPL18AP3, LINC02385, 3 more genes
    nsv5037136inversion1nstd200human GRCh38 chr12: 69,787,024-109,882,221 , GRCh37.p13 chr12: 70,180,804-110,320,026 , RPL23AP68, 540 more genes
    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
    nsv4750932insertion1nstd199human GRCh37 chr12: 104,697,281-104,697,281 , GRCh38.p12 chr12: 104,303,503-104,303,503 TXNRD1, EID3
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4456580copy number variation1nstd102humanUncertain significance GRCh37 chr12: 102,414,522-105,845,768 , GRCh38.p12 chr12: 102,020,744-105,451,990 HCFC2, MIR3652, 50 more genes
    nsv4325802inversion1nstd166human GRCh37.p13 chr12: 70,180,810-110,320,028 , GRCh38.p12 chr12: 69,787,030-109,882,223 , APAF1, 540 more genes
    nsv3924338copy number variation1nstd102humanPathogenic NCBI36 chr12: 89,962,226-108,055,398 , GRCh38 chr12: 91,044,318-109,133,210 , GRCh37 chr12: 91,438,095-109,571,015 NUP37, TTC41P, 295 more genes
    nsv3923579copy number variation1nstd102humanUncertain significance NCBI36 chr12: 102,418,033-103,644,780 , GRCh38 chr12: 103,500,125-104,726,872 , GRCh37 chr12: 103,893,903-105,120,650 LOC105369949, LINC02401, 23 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 , BTG1P1, 2451 more genes
    nsv3907610copy number variation1nstd102humanUncertain significance GRCh37 chr12: 100,580,198-105,804,075 , GRCh38.p12 chr12: 100,186,420-105,410,297 ASCL1, C12orf75-AS1, 87 more genes
    nsv3905447copy number variation2nstd102humanPathogenic GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316 , LOH12CR2, 2452 more genes
    nsv3904719copy number variation1nstd102humanPathogenic GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532 , OR5BT1P, 2441 more genes
    nsv3904242copy number variation1nstd102humanPathogenic GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309 , RNA5SP369, 2454 more genes
    nsv3897722copy number variation1nstd102humanPathogenic GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059 , RNU4ATAC16P, 2452 more genes
    nsv3897717copy number variation1nstd102humanUncertain significance GRCh37 chr12: 104,539,647-104,873,021 , GRCh38.p12 chr12: 104,145,869-104,479,243 EID3, LINC02385, 5 more genes
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