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Items: 1 to 20 of 113

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv2779041copy number variation1nstd37humanUncertain significance NCBI36 (hg18) chr2: 110,190,938-242,751,149 , GRCh37 (hg19) chr2: 110,833,649-243,102,476 , GRCh38 (hg38) chr2: 110,076,072-242,157,305 DLX2, ACVR1, 2011 more genes
    nsv2776363copy number variation2nstd37humanPathogenic GRCh37 (hg19) chr2: 12,771-242,783,384 , GRCh38 (hg38) chr2: 12,771-241,841,232 , NCBI36 (hg18) chr2: 2,771-242,432,057 DLX2, MIR561, 3855 more genes
    nsv2775081copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr2: 166,992,294-175,094,656 , GRCh37 (hg19) chr2: 167,284,048-175,386,410 , GRCh38 (hg38) chr2: 166,427,538-174,521,682 DLX2, DLX1, 117 more genes
    nsv2772356copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr2: 50,739,936-242,751,149 , GRCh37 (hg19) chr2: 50,886,432-243,102,476 , GRCh38 (hg38) chr2: 50,659,294-242,157,305 DLX2, AAMP, 3095 more genes
    nsv2771794copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr2: 169,829,974-215,521,436 , GRCh38 (hg38) chr2: 168,973,464-214,656,712 , NCBI36 (hg18) chr2: 169,538,220-215,229,681 DLX2, CHRNA1, 659 more genes
    nsv2770864copy number variation1nstd37humanUncertain significance NCBI36 (hg18) chr2: 130,861,065-242,751,149 , GRCh37 (hg19) chr2: 131,144,595-243,102,476 , GRCh38 (hg38) chr2: 130,387,022-242,157,305 DLX2, ACVR2A, 1698 more genes
    nsv2081103short tandem repeat2nstd128human GRCh37 (hg19) chr2: 172,967,129-172,967,147 , GRCh38 (hg38) chr2: 172,102,401-172,102,419 DLX2, DLX2-DT
    nsv2081102short tandem repeat2nstd128human GRCh37 (hg19) chr2: 172,967,028-172,967,049 , GRCh38 (hg38) chr2: 172,102,300-172,102,321 DLX2, DLX2-DT
    nsv2051996short tandem repeat1nstd128human GRCh37 (hg19) chr2: 172,967,770-172,967,792 , GRCh38 (hg38) chr2: 172,103,042-172,103,064 DLX2, DLX2-DT
    nsv2048197short tandem repeat11nstd128human GRCh37 (hg19) chr2: 172,974,340-172,974,385 , GRCh38 (hg38) chr2: 172,109,612-172,109,657 DLX2-DT
    nsv2048196short tandem repeat3nstd128human GRCh37 (hg19) chr2: 172,973,959-172,973,971 , GRCh38 (hg38) chr2: 172,109,231-172,109,243 DLX2-DT
    nsv2048195short tandem repeat4nstd128human GRCh37 (hg19) chr2: 172,962,294-172,962,320 , GRCh38 (hg38) chr2: 172,097,566-172,097,592 DLX2
    nsv2048058short tandem repeat2nstd128human GRCh37 (hg19) chr2: 172,971,853-172,971,876 , GRCh38 (hg38) chr2: 172,107,125-172,107,148 DLX2-DT
    nsv1194663copy number variation1nstd113human NCBI36 (hg18) chr2: 166,422,383-176,872,179 , GRCh37 (hg19) chr2: 166,714,137-177,163,933 , GRCh38 (hg38) chr2: 165,857,627-176,299,205 DLX2, ATP5MC3, 166 more genes
    nsv1190304copy number variation1nstd113human NCBI36 (hg18) chr2: 168,062,062-179,184,436 , GRCh37 (hg19) chr2: 168,353,816-179,476,191 , GRCh38 (hg38) chr2: 167,497,306-178,611,464 DLX2, ATP5MC3, 201 more genes
    nsv1189613copy number variation1nstd113human NCBI36 (hg18) chr2: 172,190,180-174,860,186 , GRCh37 (hg19) chr2: 172,481,934-175,151,940 , GRCh38 (hg38) chr2: 171,625,424-174,287,212 DLX2, ITGA6, 39 more genes
    esv3808247tandem duplication1estd192human GRCh37 (hg19) chr2: 51,280,790-211,023,500 , GRCh38 (hg38) chr2: 51,053,652-210,158,776 DLX2, PTPN18, 2502 more genes
    esv3808595copy number variation1estd192human GRCh37 (hg19) chr2: 135,855,670-180,304,688 , GRCh38 (hg38) chr2: 135,098,100-179,439,961 DLX2, HNRNPA3, 555 more genes
    esv3812160tandem duplication1estd192human GRCh37 (hg19) chr2: 5,523,755-233,845,903 , GRCh38 (hg38) chr2: 5,383,622-232,981,193 DLX2, LOC107985873, 3603 more genes
    esv3800053tandem duplication1estd192human GRCh37 (hg19) chr2: 165,592,612-200,533,317 , GRCh38 (hg38) chr2: 164,736,102-199,668,594 DLX2, HOXD1, 453 more genes
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