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Items: 1 to 20 of 22

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3317793copy number variation1nstd157human GRCh37 chr4: 134,919,721-135,184,135 , GRCh38.p12 chr4: 133,998,566-134,262,980 PABPC4L
    nsv3317802copy number variation1nstd157human GRCh37 chr8: 15,795,560-15,885,779 , GRCh38.p12 chr8: 15,938,051-16,028,270 RPL32P19
    nsv3318613copy number variation1nstd157human GRCh37 chr7: 111,059,886-111,092,478 , GRCh38.p12 chr7: 111,419,830-111,452,422 IMMP2L
    nsv3318516copy number variation22nstd157human GRCh37 chr13: 64,225,427-64,236,288 , GRCh38.p12 chr13: 63,651,294-63,662,155 LOC105370236
    nsv3317228copy number variation1nstd157human GRCh37 chr12: 82,343,280-82,349,395 , GRCh38.p12 chr12: 81,949,501-81,955,616 LINC02426
    nsv3317589copy number variation1nstd157human GRCh37 chr12: 100,260,929-100,314,359 , GRCh38.p12 chr12: 99,867,151-99,920,581 ANKS1B
    nsv3317236copy number variation1nstd157human GRCh37 chr6: 341,156-357,216 , GRCh38.p12 chr6: 341,156-357,216 DUSP22
    nsv3317595copy number variation1nstd157human GRCh37 chr3: 172,365,619-172,377,604 , GRCh38.p12 chr3: 172,647,829-172,659,814 NCEH1
    nsv3317150copy number variation3nstd157human GRCh38.p12 chr1: 103,562,368-103,587,560 , GRCh37 chr1: 104,104,990-104,130,182 AMY2B, ACTG1P4
    nsv3318690copy number variation14nstd157human GRCh38.p12 chr2: 38,733,349-38,744,481 , GRCh37 chr2: 38,960,491-38,971,623 SRSF7, GALM
    nsv3317392copy number variation23nstd157human GRCh38.p12 chr4: 68,527,638-68,623,755 , GRCh37 chr4: 69,393,356-69,489,473 UGT2B17, LOC100132651, 1 more genes
    nsv3318503copy number variation1nstd157human GRCh37 chr17: 41,341,984-41,375,597 , GRCh38.p12 chr17: 43,189,967-43,223,574 NBR1, TMEM106A, 1 more genes
    nsv3317327copy number variation24nstd157human GRCh38.p12 chr2: 241,911,938-242,092,368 , GRCh37 chr2: 242,854,089-243,034,519 , GRCh38.p12 chr2|NT_187647.1: 1-136,078 , GRCh38.p12 chr2|NT_187523.1: 1-136,438 LOC285097, LINC01881, 4 more genes
    nsv3317442copy number variation7nstd157human GRCh37 chr4: 161,048,496-161,072,119 , GRCh38.p12 chr4: 160,127,344-160,150,967 0
    nsv3317859copy number variation29nstd157human GRCh37 chr4: 64,136,609-64,154,477 , GRCh38.p12 chr4: 63,270,891-63,288,759 0
    nsv3317324copy number variation1nstd157human GRCh37 chr1: 106,921,365-106,938,598 , GRCh38.p12 chr1: 106,378,743-106,395,976 0
    nsv3318427copy number variation34nstd157human GRCh37 chr11: 81,501,218-81,517,261 , GRCh38.p12 chr11: 81,790,176-81,806,219 0
    nsv3318432copy number variation41nstd157human GRCh37 chr8: 5,595,511-5,605,706 , GRCh38.p12 chr8: 5,737,989-5,748,184 0
    nsv3318956copy number variation1nstd157human GRCh37 chr21: 21,591,443-21,600,723 , GRCh38.p12 chr21: 20,219,130-20,228,410 0
    nsv3318502copy number variation31nstd157human GRCh37 chr9: 78,004,378-78,011,616 , GRCh38.p12 chr9: 75,389,462-75,396,700 0
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