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Items: 1 to 20 of 3069

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3600181copy number variation743estd214human GRCh37 chr4: 34,781,317-34,849,886 , GRCh38.p12 chr4: 34,779,695-34,848,264 , GRCh38.p12 chr4|NW_003315915.1: 272,024-340,593 LOC105378262
    esv3600180copy number variation743estd214human GRCh37 chr4: 34,779,933-34,828,997 , GRCh38.p12 chr4|NW_003315915.1: 270,640-319,704 , GRCh38.p12 chr4: 34,778,311-34,827,375 LOC105378262
    esv3587491copy number variation2473estd214human GRCh37 chr1: 149,531,789-149,573,452 , GRCh38.p12 chr1: 120,868,540-120,910,198 PPIAL4A
    esv3644983copy number variation2409estd214human GRCh37 chr20: 1,559,739-1,594,685 , GRCh38.p12 chr20: 1,579,093-1,614,039 SIRPB1
    esv3625569copy number variation56estd214human GRCh37 chr11: 21,186,933-21,217,159 , GRCh38.p12 chr11: 21,165,387-21,195,613 NELL1
    esv3632214copy number variation1037estd214human GRCh37 chr13: 57,752,516-57,781,577 , GRCh38.p12 chr13: 57,178,382-57,207,443 MTCO2P3
    esv3588471copy number variation1062estd214human GRCh37 chr1: 196,735,895-196,764,940 , GRCh38.p12 chr1: 196,766,765-196,795,810 CFHR3
    esv3600875copy number variation1672estd214human GRCh37 chr4: 69,425,939-69,455,053 , GRCh38.p12 chr4: 68,560,221-68,589,335 UGT2B17
    esv3623922copy number variation1739estd214human GRCh37 chr10: 81,474,561-81,502,396 , GRCh38.p12 chr10: 79,714,805-79,742,640 NUTM2B-AS1
    esv3598490copy number variation4estd214human GRCh37 chr3: 164,523,774-164,551,589 , GRCh38.p12 chr3: 164,805,986-164,833,801 LINC01324
    esv3607280copy number variation95estd214human GRCh37 chr5: 155,566,445-155,591,598 , GRCh38.p12 chr5: 156,139,435-156,164,588 SGCD
    esv3603772copy number variation1611estd214human GRCh37 chr5: 757,676-778,933 , GRCh38.p12 chr5: 757,561-778,818 ZDHHC11B
    esv3632088copy number variation270estd214human GRCh37 chr13: 52,882,403-52,902,898 , GRCh38.p12 chr13: 52,308,268-52,328,763 TPTE2P2
    esv3615450copy number variation178estd214human GRCh37 chr7: 149,862,878-149,883,330 , GRCh38.p12 chr7: 150,165,789-150,186,241 ACTR3C
    esv3591709copy number variation1476estd214human GRCh37 chr2: 98,136,216-98,156,567 , GRCh38.p12 chr2: 97,519,753-97,540,104 ANKRD36B
    esv3625301copy number variation552estd214human GRCh37 chr11: 7,812,280-7,832,579 , GRCh38.p12 chr11: 7,790,733-7,811,032 , GRCh38.p12 chr11|NW_011332695.1: 11,601-31,902 , GRCh38.p12 chr11|NT_187583.1: 11,601-31,900 OR5P2
    esv3628470copy number variation4908estd214human GRCh37 chr12: 8,568,920-8,587,027 , GRCh38.p12 chr12: 8,416,324-8,434,431 OR7E148P
    esv3612805copy number variation54estd214human GRCh37 chr7: 34,895,675-34,913,807 , GRCh38.p12 chr7: 34,856,063-34,874,195 NPSR1
    esv3623140copy number variation1029estd214human GRCh37 chr10: 47,983,067-48,000,904 , GRCh38.p12 chr10: 50,168,602-50,186,441 ASAH2
    esv3648066copy number variation1estd214human GRCh37 chr22: 50,030,103-50,048,669 , GRCh38.p12 chr22: 49,636,455-49,655,021 MIR3667HG
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