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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3873055copy number variation1nstd102humanBenign GRCh37 chr6: 26,433,329-26,460,721 , GRCh38.p12 chr6: 26,433,101-26,460,493 BTN3A3, BTN2A1
    nsv3888049copy number variation1nstd102humanBenign GRCh37 chr6: 26,433,329-26,459,244 , GRCh38.p12 chr6: 26,433,101-26,459,016 BTN3A3, BTN2A1
    nsv3887400copy number variation1nstd102humanBenign GRCh37 chr6: 26,440,542-26,459,961 , GRCh38.p12 chr6: 26,440,314-26,459,733 BTN3A3, BTN2A1
    nsv3879990copy number variation1nstd102humanBenign GRCh37 chr6: 26,369,549-26,442,786 , GRCh38.p12 chr6: 26,369,321-26,442,558 BTN3A1, BTN3A3, 3 more genes
    nsv3877479copy number variation1nstd102humanBenign GRCh37 chr6: 26,428,062-26,462,877 , GRCh38.p12 chr6: 26,427,834-26,462,649 BTN2A3P, BTN2A1, 1 more genes
    nsv4456851copy number variation1nstd102humanUncertain significance GRCh37 chr6: 26,366,119-26,444,946 , GRCh38.p12 chr6: 26,365,891-26,444,718 BTN3A3, BTN2A3P, 3 more genes
    nsv4456432copy number variation1nstd102humanUncertain significance GRCh37 chr6: 26,366,119-26,444,945 , GRCh38.p12 chr6: 26,365,891-26,444,717 BTN3A1, BTN3A3, 3 more genes
    nsv3889848copy number variation1nstd102humanPathogenic GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719 BTF3, MEGF10, 2080 more genes
    nsv3886374copy number variation1nstd102humanPathogenic GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028 BTF3, LOC105374618, 2499 more genes
    nsv3871533copy number variation1nstd102humanPathogenic GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343 BTF3, PCDHGC5, 2492 more genes
    nsv3875235copy number variation2nstd102humanPathogenic GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788 BTF3, SPEF2, 2490 more genes
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 LOC105378061, MIR4640, 2914 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 RNU6-411P, LOC107986611, 2910 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 SOD1P1, HLA-DPB1, 2905 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 ITPR3, HSD17B8, 2905 more genes
    nsv3911585copy number variation1nstd102humanPathogenic NCBI36 chr5: 75,149-73,744,306 , GRCh38 chr5: 22,149-74,412,725 , GRCh37 chr5: 22,149-73,708,550 BTF3, LINC02241, 878 more genes
    nsv3913920copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028 TRR-ACG1-2, TMEM217, 1385 more genes
    nsv3920564copy number variation1nstd102humanPathogenic GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946 PRELID1P2, RPL7AP7, 785 more genes
    nsv4675667copy number variation1nstd102humanPathogenic GRCh37 chr5: 72,790,061-97,478,870 , GRCh38.p12 chr5: 73,494,236-98,143,166 BTF3, LOC101929380, 318 more genes
    nsv4578696copy number variation1nstd102humanLikely pathogenic GRCh38 chr5: 58,780,641-73,523,380 , GRCh37.p13 chr5: 58,076,468-72,819,205 BTF3, TRIM23, 215 more genes
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