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Items: 1 to 20 of 86

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4993699copy number variation1nstd200human GRCh38 chr12: 113,156,642-113,239,842 , GRCh37.p13 chr12: 113,594,447-113,677,647 IQCD, MIR7106, 4 more genes
    nsv4839363copy number variation1nstd200human GRCh37 chr12: 113,594,447-113,677,647 , GRCh38.p12 chr12: 113,156,642-113,239,842 IQCD, TPCN1, 4 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
    nsv3914285copy number variation1nstd102humanPathogenic GRCh38 chr12: 113,077,775-114,372,366 , NCBI36 chr12: 111,999,963-113,294,554 , GRCh37 chr12: 113,515,580-114,810,171 RITA1, DTX1, 27 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
    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
    nsv3902071copy number variation1nstd102humanBenign GRCh37 chr12: 113,466,061-113,596,866 , GRCh38.p12 chr12: 113,028,256-113,159,061 DTX1, RPS15AP32, 4 more genes
    nsv3897722copy number variation1nstd102humanPathogenic GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059 , RNU4ATAC16P, 2452 more genes
    nsv3169098inversion1nstd158human GRCh37 chr12: 28,095,967-121,612,723 , GRCh38.p12 chr12: 27,943,034-121,174,920 , ACACB, 1642 more genes
    nsv3168340inversion1nstd158human GRCh37 chr12: 66,451,836-123,782,201 , GRCh38.p12 chr12: 66,058,056-123,297,654 , ACACB, 909 more genes
    nsv3156916copy number variation1nstd151human GRCh37 chr12: 113,495,995-113,909,308 , GRCh38.p12 chr12: 113,058,190-113,471,503 , SDS, 15 more genes
    nsv3155398copy number variation1nstd151human GRCh37 chr12: 113,552,602-113,599,807 , GRCh38.p12 chr12: 113,114,797-113,162,002 DDX54, RASAL1, 2 more genes
    nsv3141418copy number variation1nstd151human GRCh37 chr12: 113,532,591-113,714,845 , GRCh38.p12 chr12: 113,094,786-113,277,040 DDX54, RITA1, 6 more genes
    nsv3140885copy number variation1nstd151human GRCh37 chr12: 113,565,614-113,664,774 , GRCh38.p12 chr12: 113,127,809-113,226,969 TPCN1, CFAP73, 5 more genes
    nsv2740531copy number variation1nstd130human NCBI36 chr12: 49,559,698-128,874,436 , GRCh37.p13 chr12: 51,273,431-130,308,483 , GRCh38.p12 chr12: 50,879,648-129,823,938 , LINC01234, 1477 more genes
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