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Items: 1 to 20 of 195

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5954674insertion1nstd209human GRCh38 chr1: 27,107,220-27,107,220 , GRCh37.p13 chr1: 27,433,711-27,433,711 SLC9A1
    nsv5886725copy number variation1nstd209human GRCh38 chr1: 27,138,377-27,139,616 , GRCh37.p13 chr1: 27,464,868-27,466,107 SLC9A1
    nsv5829673copy number variation1nstd209human GRCh38 chr1: 27,138,269-27,139,868 , GRCh37.p13 chr1: 27,464,760-27,466,359 SLC9A1
    nsv5728937mobile element insertion1nstd211human GRCh38 chr1: 27,097,823-27,097,823 , GRCh37.p13 chr1: 27,424,314-27,424,314 SLC9A1
    nsv5611963insertion1nstd207human GRCh38 chr1: 27,107,220-27,107,220 , GRCh37.p13 chr1: 27,433,711-27,433,711 SLC9A1
    nsv5427686copy number variation1nstd206human GRCh38 chr1: 22,064,395-28,290,354 , GRCh37.p13 chr1: 22,390,888-28,616,865 , NCMAP-DT, 201 more genes
    nsv5424026copy number variation1nstd206human GRCh38 chr1: 27,144,197-27,144,375 , GRCh37.p13 chr1: 27,470,688-27,470,866 SLC9A1
    nsv5421185copy number variation1nstd206human GRCh38 chr1: 27,133,034-27,133,091 , GRCh37.p13 chr1: 27,459,525-27,459,582 SLC9A1
    nsv5419195copy number variation1nstd206human GRCh38 chr1: 27,138,379-27,139,617 , GRCh37.p13 chr1: 27,464,870-27,466,108 SLC9A1
    nsv5350646translocation1nstd200human GRCh38 chr1: 27,138,379-27,138,379 , GRCh38 chr1: 27,139,617-27,139,617 , GRCh37.p13 chr1: 27,466,108-27,466,108 , GRCh37.p13 chr1: 27,464,870-27,464,870 SLC9A1
    nsv5337283translocation1nstd200human GRCh37 chr1: 27,464,870-27,464,870 , GRCh37 chr1: 27,466,108-27,466,108 , GRCh38.p12 chr1: 27,138,379-27,138,379 , GRCh38.p12 chr1: 27,139,617-27,139,617 SLC9A1
    nsv5295634copy number variation1nstd204human GRCh38.p13 chr1: 27,120,507-27,121,894 , GRCh37.p13 chr1: 27,446,998-27,448,385 SLC9A1
    nsv5209067copy number variation1nstd204human GRCh38.p13 chr1: 27,087,001-28,123,900 , GRCh37.p13 chr1: 27,413,492-28,450,411 LOC729973, IFI6, 38 more genes
    nsv5206193copy number variation1nstd204human GRCh38.p13 chr1: 26,819,201-27,230,300 , GRCh37.p13 chr1: 27,145,692-27,556,791 KDF1, RPL12P13, 18 more genes
    nsv5075515mobile element insertion1nstd203human GRCh38 chr1: 27,147,275-27,147,299 , GRCh37.p13 chr1: 27,473,766-27,473,790 SLC9A1
    nsv4903248copy number variation1nstd200human GRCh38 chr1: 27,105,275-27,123,698 , GRCh37.p13 chr1: 27,431,766-27,450,189 SLC9A1
    nsv4788607copy number variation1nstd200human GRCh37 chr1: 27,447,025-27,448,357 , GRCh38.p12 chr1: 27,120,534-27,121,866 SLC9A1
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4761183inversion1nstd199human GRCh37 chr1: 16,884,570-145,374,569 , GRCh38.p12 chr1: 16,558,075-149,528,945 , ABCA4, 2341 more genes
    nsv4760635insertion1nstd199human GRCh37 chr1: 27,433,627-27,433,627 , GRCh38.p12 chr1: 27,107,136-27,107,136 SLC9A1
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