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Items: 1 to 20 of 2824

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3621845copy number variation340estd214human GRCh37 chr9: 132,654,988-132,798,900 , GRCh38.p12 chr9: 129,892,709-130,036,621 FNBP1
    esv3637117copy number variation139estd214human GRCh37 chr15: 86,064,810-86,182,627 , GRCh38.p12 chr15: 85,521,579-85,639,396 AKAP13
    esv3604168copy number variation41estd214human GRCh37 chr5: 17,526,853-17,606,025 , GRCh38.p12 chr5: 17,526,744-17,605,916 TAF11L6
    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
    esv3616948copy number variation1095estd214human GRCh37 chr8: 39,231,505-39,288,323 , GRCh38.p12 chr8: 39,373,986-39,430,804 ADAM5
    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
    esv3596068copy number variation520estd214human GRCh37 chr3: 46,803,577-46,851,159 , GRCh38.p12 chr3: 46,762,087-46,809,669 PRSS44P
    esv3606289copy number variation3estd214human GRCh37 chr5: 111,438,045-111,484,253 , GRCh38.p12 chr5: 112,102,348-112,148,556 EPB41L4A
    esv3598497copy number variation28estd214human GRCh37 chr3: 165,039,860-165,084,371 , GRCh38.p12 chr3: 165,322,072-165,366,583 LINC01322
    esv3587491copy number variation2473estd214human GRCh37 chr1: 149,531,789-149,573,452 , GRCh38.p12 chr1: 120,868,540-120,910,198 PPIAL4A
    esv3606288copy number variation2estd214human GRCh37 chr5: 111,438,237-111,476,444 , GRCh38.p12 chr5: 112,102,540-112,140,747 EPB41L4A
    esv3593815copy number variation31estd214human GRCh37 chr2: 194,578,564-194,613,101 , GRCh38.p12 chr2: 193,713,840-193,748,377 SEC61GP1
    esv3644983copy number variation2409estd214human GRCh37 chr20: 1,559,739-1,594,685 , GRCh38.p12 chr20: 1,579,093-1,614,039 SIRPB1
    esv3633539copy number variation8estd214human GRCh37 chr13: 110,732,474-110,761,471 , GRCh38.p12 chr13: 110,080,127-110,109,124 RN7SL783P
    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
    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
    esv3633541copy number variation8estd214human GRCh37 chr13: 110,740,960-110,763,627 , GRCh38.p12 chr13: 110,088,613-110,111,280 RN7SL783P
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