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Items: 9

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    Number of Variants: 9

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6630626copy number variation240nstd224human GRCh37 chr5: 97,061,761-97,096,042 , GRCh38.p12 chr5: 97,726,057-97,760,338 LOC391813
    nsv6621231copy number variation29nstd224human GRCh37 chr11: 95,569,341-95,621,376 , GRCh38.p12 chr11: 95,836,177-95,888,212 MTMR2, RNA5SP345
    nsv6629125copy number variation1nstd224human GRCh37 chr4: 148,722,083-148,897,030 , GRCh38.p12 chr4: 147,800,932-147,975,879 RFPL4AP4, RN7SL254P, 1 more genes
    nsv6625917copy number variation63nstd224human GRCh37 chr1: 17,216,331-17,266,464 , GRCh38.p12 chr1: 16,889,836-16,939,969 CROCC, LOC105376805, 3 more genes
    nsv6628186copy number variation71nstd224human GRCh37 chr3: 100,351,696-100,427,937 , GRCh38.p12 chr3: 100,632,852-100,709,093 TFG, ADGRG7, 1 more genes
    nsv6631445copy number variation586nstd224human GRCh37 chr6: 67,017,543-67,044,431 , GRCh38.p12 chr6: 66,307,650-66,334,538 0
    nsv6621601copy number variation56nstd224human GRCh37 chr12: 31,296,219-31,406,907 , GRCh38.p12 chr12: 31,143,285-31,253,973 , GRCh38.p12 chr12|NT_187587.1: 34,079-144,767 OVOS2, RPL13AP22, 5 more genes
    nsv6631164copy number variation1nstd224human GRCh37 chr6: 31,963,844-32,011,639 , GRCh38.p12 chr6: 31,996,067-32,043,862 C4A, C4B, 5 more genes
    nsv6632147copy number variation132nstd224human GRCh37 chr7: 44,935-67,365 , GRCh38.p12 chr7: 44,935-67,365 , GRCh38.p12 chr7|NT_187558.1: 1,034-23,464 , GRCh38.p12 chr7|NT_187653.1: 37,256-59,686 0
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