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Items: 1 to 20 of 2779

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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
    esv3600875copy number variation1672estd214human GRCh37 chr4: 69,425,939-69,455,053 , GRCh38.p12 chr4: 68,560,221-68,589,335 UGT2B17
    esv3591237copy number variation10estd214human GRCh37 chr2: 72,248,420-72,277,337 , GRCh38.p12 chr2: 72,021,290-72,050,207 LOC105374798
    esv3623922copy number variation1739estd214human GRCh37 chr10: 81,474,561-81,502,396 , GRCh38.p12 chr10: 79,714,805-79,742,640 NUTM2B-AS1
    esv3615267copy number variation544estd214human GRCh37 chr7: 141,765,307-141,792,849 , GRCh38.p12 chr7: 142,065,507-142,093,049 , GRCh38.p12 chr7|NT_187562.1: 27,387-54,929 MGAM
    esv3620473copy number variation1254estd214human GRCh37 chr9: 43,580,844-43,606,160 , GRCh38.p12 chr9: 42,208,229-42,233,545 LOC112268036
    esv3638686copy number variation852estd214human GRCh37 chr16: 55,798,890-55,822,423 , GRCh38.p12 chr16: 55,764,978-55,788,511 CES1P1
    esv3603772copy number variation1611estd214human GRCh37 chr5: 757,676-778,933 , GRCh38.p12 chr5: 757,561-778,818 ZDHHC11B
    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
    esv3587880copy number variation879estd214human GRCh37 chr1: 169,224,713-169,245,824 , GRCh38.p12 chr1: 169,255,475-169,276,586 NME7
    esv3628470copy number variation4908estd214human GRCh37 chr12: 8,568,920-8,587,027 , GRCh38.p12 chr12: 8,416,324-8,434,431 OR7E148P
    esv3636072copy number variation227estd214human GRCh37 chr15: 32,504,287-32,519,739 , GRCh38.p12 chr15: 32,212,086-32,227,538 LOC102724078
    esv3817576copy number variation14estd214human GRCh37 chrX: 130,778,541-130,793,464 , GRCh38.p12 chrX: 131,644,538-131,659,451 HDGFP1
    esv3606364copy number variation16estd214human GRCh37 chr5: 114,706,220-114,721,108 , GRCh38.p12 chr5: 115,370,523-115,385,411 LOC105379130
    esv3620460copy number variation1877estd214human GRCh37 chr9: 41,971,191-41,985,717 , GRCh38.p12 chr9: 39,826,173-39,840,699 FGF7P3
    esv3644676copy number variation1486estd214human GRCh37 chr19: 52,134,835-52,149,093 , GRCh38.p12 chr19: 51,631,582-51,645,840 SIGLEC14
    esv3599249copy number variation624estd214human GRCh37 chr3: 195,456,936-195,471,412 , GRCh38.p12 chr3|NT_187689.1: 100,562-115,038 , GRCh38.p12 chr3|NT_187532.1: 100,562-115,038 , GRCh38.p12 chr3|NT_187649.1: 50,164-64,603 , GRCh38.p12 chr3|NT_187690.1: 50,159-64,610 , GRCh38.p12 chr3|NT_187691.1: 50,266-64,780 , GRCh38.p12 chr3|NT_187688.1: 50,160-64,603 , GRCh38.p12 chr3: 195,730,065-195,744,541 , GRCh38.p12 chr3|NT_187678.1: 51,460-65,948 MUC20
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