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Items: 1 to 20 of 3763

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2745334copy number variation162estd201human GRCh37 chr11: 134,354,170-134,474,375 , GRCh38.p12 chr11: 134,484,276-134,604,481 B3GAT1-DT
    esv2735675copy number variation87estd201human GRCh37 chr7: 157,080,963-157,195,991 , GRCh38.p12 chr7: 157,288,269-157,403,297 DNAJB6
    esv2723905copy number variation22estd201human GRCh37 chr1: 225,755,130-225,840,341 , GRCh38.p12 chr1: 225,567,428-225,652,639 ENAH
    esv2720097copy number variation20estd201human GRCh37 chr2: 56,738,645-56,818,080 , GRCh38.p12 chr2: 56,511,510-56,590,945 LOC101927213
    esv2733876copy number variation75estd201human GRCh37 chr7: 3,708,209-3,765,709 , GRCh38.p12 chr7: 3,668,577-3,726,077 SDK1
    esv2730962copy number variation6estd201human GRCh37 chr10: 2,622,225-2,678,722 , GRCh38.p12 chr10: 2,580,033-2,636,530 LOC105376350
    esv2723060copy number variation156estd201human GRCh37 chr21: 10,472,498-10,528,469 , GRCh38.p12 chr21: 9,994,470-10,050,441 LOC105372733
    esv2738432copy number variation22estd201human GRCh37 chr9: 37,053,917-37,100,460 , GRCh38.p12 chr9: 37,053,920-37,100,463 EBLN3P
    esv2720361copy number variation324estd201human GRCh37 chr1: 2,583,966-2,628,877 , GRCh38.p12 chr1|NT_187515.1: 219,010-258,013 , GRCh38.p12 chr1: 2,652,527-2,697,438 TTC34
    esv2720584copy number variation301estd201human GRCh37 chr1: 2,583,971-2,628,877 , GRCh38.p12 chr1|NT_187515.1: 219,010-258,013 , GRCh38.p12 chr1: 2,652,532-2,697,438 TTC34
    esv2720806copy number variation265estd201human GRCh37 chr1: 2,584,075-2,628,877 , GRCh38.p12 chr1|NT_187515.1: 219,010-258,013 , GRCh38.p12 chr1: 2,652,636-2,697,438 TTC34
    esv2721028copy number variation255estd201human GRCh37 chr1: 2,584,101-2,628,877 , GRCh38.p12 chr1: 2,652,662-2,697,438 , GRCh38.p12 chr1|NT_187515.1: 219,010-258,013 TTC34
    esv2720139copy number variation274estd201human GRCh37 chr1: 2,583,492-2,620,302 , GRCh38.p12 chr1|NT_187515.1: 219,010-249,438 , GRCh38.p12 chr1: 2,652,053-2,688,863 TTC34
    esv2735255copy number variation70estd201human GRCh37 chr7: 141,751,744-141,786,850 , GRCh38.p12 chr7: 142,051,944-142,087,050 , GRCh38.p12 chr7|NT_187562.1: 13,824-48,930 MGAM
    esv2722072copy number variation80estd201human GRCh37 chr20: 1,561,011-1,594,167 , GRCh38.p12 chr20: 1,580,365-1,613,521 SIRPB1
    esv2739857copy number variation87estd201human GRCh37 chrX: 2,365,622-2,398,182 , GRCh38.p12 chrX: 2,447,581-2,480,141 DHRSX
    esv2740148copy number variation21estd201human GRCh37 chrX: 48,068,038-48,097,849 , GRCh38.p12 chrX: 48,208,603-48,238,414 S100A11P7
    esv2742587copy number variation1estd201human GRCh37 chr7: 141,768,859-141,797,711 , GRCh38.p12 chr7: 142,069,059-142,097,911 , GRCh38.p12 chr7|NT_187562.1: 30,939-59,791 MGAM
    esv2744176copy number variation107estd201human GRCh37 chr11: 18,957,902-18,986,343 , GRCh38.p12 chr11: 18,936,355-18,964,796 MRGPRX11P
    esv2743978copy number variation96estd201human GRCh37 chr11: 1,915,287-1,936,956 , GRCh38.p12 chr11: 1,894,057-1,915,726 LINC01150
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