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Items: 1 to 20 of 1697

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1077919copy number variation1nstd99human GRCh37 chr21: 10,770,599-10,893,300 , GRCh38.p12 chr21: 10,619,157-10,741,858 IGHV1OR21-1
    nsv1076328copy number variation1nstd99human GRCh37 chr1: 142,874,399-142,967,700 , GRCh38.p12 chrUn|NT_187513.1: 93,377-186,678 LOC105379566
    nsv1077505copy number variation1nstd99human GRCh37 chr8: 2,195,099-2,284,800 , GRCh38.p12 chr8|NT_187576.1: 430,309-520,010 LOC105377783
    nsv1077964copy number variation1nstd99human GRCh37 chr4: 49,093,199-49,173,300 , GRCh38.p12 chr4: 49,091,182-49,171,283 LOC101927209
    nsv1076363copy number variation1nstd99human GRCh37 chr10: 42,608,699-42,687,300 , GRCh38.p12 chr10: 42,113,251-42,191,852 , GRCh38.p12 chr10|NT_187579.1: 10,012-89,655 KSR1P1
    nsv1077874copy number variation1nstd99human GRCh37 chr2: 90,371,499-90,447,500 , GRCh38.p12 chr2: 90,326,537-90,402,511 0
    nsv1077551copy number variation1nstd99human GRCh37 chr9: 68,446,599-68,514,000 , GRCh38.p12 chr9: 63,850,865-63,918,266 FRG1JP
    nsv1078720copy number variation1nstd99human GRCh37 chrY: 58,967,699-59,033,100 , GRCh38.p12 chrY: 56,821,552-56,886,953 , GRCh38.p12 chrY|NW_009646209.1: 34,800-100,201 CTBP2P1
    nsv1077453copy number variation1nstd99human GRCh37 chr5: 21,507,999-21,573,400 , GRCh38.p12 chr5: 21,507,890-21,573,291 GUSBP1
    nsv1075874copy number variation1nstd99human GRCh37 chr15: 20,024,099-20,088,700 , GRCh38.p12 chr15: 19,818,846-19,883,447 RNU6-978P
    nsv1076442copy number variation1nstd99human GRCh37 chr17: 21,193,699-21,254,600 , GRCh38.p12 chr17: 21,290,387-21,351,288 MAP2K3
    nsv1075378copy number variation1nstd99human GRCh37 chr1: 143,461,899-143,522,500 , GRCh38.p12 chr14|NT_113796.3: 119,083-179,684 LOC105379271
    nsv1076402copy number variation1nstd99human GRCh37 chr14: 19,066,099-19,126,000 , GRCh38.p12 chr14: 18,289,622-18,349,523 RNU6-458P
    nsv1076597copy number variation1nstd99human GRCh37 chr6: 57,321,899-57,423,100 , GRCh38.p12 chr3: 91,458,843-91,516,820 , GRCh38.p12 chr3|NW_009646198.1: 211,504-269,480
    nsv1076599copy number variation1nstd99human GRCh37 chr6: 57,478,899-57,533,200 , GRCh38.p12 chr6: 60,511,152-60,565,453 PRIM2BP
    nsv1077310copy number variation1nstd99human GRCh37 chr1: 206,482,899-206,534,400 , GRCh38.p12 chr1: 206,309,555-206,361,045 SRGAP2
    nsv1077781copy number variation1nstd99human GRCh37 chr14: 20,023,099-20,072,100 , GRCh38.p12 chr14: 18,915,606-18,964,607 MED15P6
    nsv1075814copy number variation1nstd99human GRCh37 chr10: 38,868,899-38,914,300 , GRCh38.p12 chr10: 38,575,768-38,621,169 ABCD1P2
    nsv1077904copy number variation1nstd99human GRCh37 chr20: 25,858,699-25,902,600 , GRCh38.p12 chr20: 25,878,063-25,921,964 CFTRP1
    nsv1077431copy number variation1nstd99human GRCh37 chr4: 3,569,699-3,612,100 , GRCh38.p12 chr4: 3,567,972-3,610,373 LINC00955
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