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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098877copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 80,187,643-80,222,244 , GRCh38.p12 chr12: 79,793,863-79,828,464 PPP1R12A
    nsv3896942copy number variation1nstd102humanBenign GRCh37 chr12: 80,134,746-80,163,079 , GRCh38.p12 chr12: 79,740,966-79,769,299 PPP1R12A-AS2
    nsv3896099copy number variation1nstd102humanBenign GRCh37 chr12: 80,141,400-80,163,079 , GRCh38.p12 chr12: 79,747,620-79,769,299 PPP1R12A-AS2
    nsv3898399copy number variation1nstd102humanBenign GRCh37 chr12: 80,141,400-80,162,316 , GRCh38.p12 chr12: 79,747,620-79,768,536 PPP1R12A-AS2
    nsv3897496copy number variation1nstd102humanBenign GRCh37 chr12: 80,155,109-80,163,528 , GRCh38.p12 chr12: 79,761,329-79,769,748 PPP1R12A-AS2
    nsv3901573copy number variation1nstd102humanBenign GRCh37 chr12: 80,155,109-80,163,079 , GRCh38.p12 chr12: 79,761,329-79,769,299 PPP1R12A-AS2
    nsv5380732copy number variation1nstd102humannot provided GRCh38 chr12: 79,761,819-79,761,820 , GRCh37 chr12: 80,155,599-80,155,600 PPP1R12A-AS2
    esv3648644copy number variation1estd216humannot provided GRCh38.p12 chr12: 79,761,820-79,766,450 , GRCh37 chr12: 80,155,600-80,160,230 PPP1R12A-AS2
    nsv3891563copy number variation1nstd102humanBenign GRCh37 chr12: 80,116,407-80,208,853 , GRCh38.p12 chr12: 79,722,627-79,815,073 PPP1R12A, PPP1R12A-AS2
    nsv7093980copy number variation1nstd102humanLikely benign GRCh37 chr12: 80,169,709-80,215,990 , GRCh38.p12 chr12: 79,775,929-79,822,210 PPP1R12A, PPP1R12A-AS2
    nsv3895148copy number variation1nstd102humanBenign GRCh37 chr12: 80,155,109-80,168,660 , GRCh38.p12 chr12: 79,761,329-79,774,880 PPP1R12A, PPP1R12A-AS2
    nsv7094054copy number variation1nstd102humanPathogenic GRCh37 chr12: 80,239,062-80,328,711 , GRCh38.p12 chr12: 79,845,282-79,934,931 PPP1R12A, RNA5SP363, 1 more genes
    nsv4456995copy number variation1nstd102humanUncertain significance GRCh37 chr12: 79,732,756-80,116,407 , GRCh38.p12 chr12: 79,338,976-79,722,627 SYT1, NOP56P3, 3 more genes
    nsv3892030copy number variation1nstd102humanPathogenic GRCh37 chr12: 69,608,090-89,629,345 , GRCh38.p12 chr12: 69,214,310-89,235,568 PPP1R12A, LOC101928002, 197 more genes
    nsv3922777copy number variation1nstd102humanPathogenic GRCh37 chr12: 73,879,477-93,189,581 , NCBI36 chr12: 72,165,744-91,713,712 , GRCh38 chr12: 73,485,697-92,795,805 PPP1R12A, RN7SL734P, 195 more genes
    nsv4456763copy number variation1nstd102humanPathogenic GRCh37 chr12: 77,737,623-94,330,526 , GRCh38.p12 chr12: 77,343,843-93,936,750 PPP1R12A, MIR1252, 162 more genes
    nsv3924329copy number variation1nstd102humanPathogenic GRCh37 chr12: 70,731,264-82,154,924 , GRCh38 chr12: 70,337,484-81,761,145 , NCBI36 chr12: 69,017,531-80,679,055 PPP1R12A, NAV3, 118 more genes
    nsv3918758copy number variation1nstd102humanPathogenic GRCh38 chr12: 75,683,698-80,195,649 , NCBI36 chr12: 74,363,745-79,113,560 , GRCh37 chr12: 76,077,478-80,589,429 PPP1R12A, YWHAQP7, 48 more genes
    nsv3904242copy number variation1nstd102humanPathogenic GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309 PPP1R12A, RNA5SP369, 2454 more genes
    nsv3905447copy number variation2nstd102humanPathogenic GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316 PPP1R12A, LOH12CR2, 2452 more genes
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