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Items: 1 to 20 of 138

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5903293copy number variation1nstd209human GRCh38 chr2: 121,734,749-121,734,806 , GRCh37.p13 chr2: 122,492,325-122,492,382 NIFK
    nsv5558142mobile element insertion1nstd206human GRCh38 chr2: 102,295,972-141,288,199 , GRCh37.p13 chr2: 102,912,432-142,045,768 , LOC105373587, 623 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5436164copy number variation1nstd206human GRCh38 chr2: 121,734,750-121,734,807 , GRCh37.p13 chr2: 122,492,326-122,492,383 NIFK
    nsv5435862copy number variation1nstd206human GRCh38 chr2: 121,558,631-122,131,082 , GRCh37.p13 chr2: 122,316,207-122,888,658 TSN, CLASP1, 7 more genes
    nsv5293635copy number variation1nstd204human GRCh38.p13 chr2: 121,688,163-121,741,660 , GRCh37.p13 chr2: 122,445,739-122,499,236 NPM1P32, NIFK, 1 more genes
    nsv5212540copy number variation1nstd204human GRCh38.p13 chr2: 121,728,071-121,740,600 , GRCh37.p13 chr2: 122,485,647-122,498,176 NIFK-AS1, NIFK
    nsv5205058copy number variation1nstd204human GRCh38.p13 chr2: 121,688,701-121,741,200 , GRCh37.p13 chr2: 122,446,277-122,498,776 NIFK, NIFK-AS1, 1 more genes
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv5033955inversion1nstd200human GRCh38 chr2: 103,800,446-187,202,765 , GRCh37.p13 chr2: 104,416,904-188,067,492 , EDDM3CP, 1184 more genes
    nsv4923910copy number variation1nstd200human GRCh38 chr2: 121,688,545-121,741,330 , GRCh37.p13 chr2: 122,446,121-122,498,906 NPM1P32, NIFK-AS1, 1 more genes
    nsv4923907copy number variation1nstd200human GRCh38 chr2: 121,419,207-121,790,651 , GRCh37.p13 chr2: 122,176,783-122,548,227 LOC105373590, RPL12P15, 8 more genes
    nsv4915332copy number variation1nstd200human GRCh38 chr2: 121,729,313-121,730,391 , GRCh37.p13 chr2: 122,486,889-122,487,967 NIFK
    nsv4879764inversion1nstd200human GRCh37 chr2: 104,416,904-188,067,492 , GRCh38.p12 chr2: 103,800,446-187,202,765 , ACMSD, 1184 more genes
    nsv4781754copy number variation1nstd200human GRCh37 chr2: 122,446,121-122,498,906 , GRCh38.p12 chr2: 121,688,545-121,741,330 NPM1P32, NIFK, 1 more genes
    nsv4770609copy number variation1nstd200human GRCh37 chr2: 122,486,887-122,487,967 , GRCh38.p12 chr2: 121,729,311-121,730,391 NIFK
    nsv4743379copy number variation1nstd199human GRCh37 chr2: 88,481,090-124,440,189 , GRCh38.p12 chr9: 40,649,751-63,450,622 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 88,181,571-123,682,613 , EIF2AK3, 861 more genes
    nsv4674739copy number variation1nstd102humanPathogenic GRCh37 chr2: 118,903,294-123,099,547 , GRCh38.p12 chr2: 118,145,718-122,341,971 LOC101927709, NIFK-AS1, 55 more genes
    nsv4674710copy number variation1nstd102humanPathogenic GRCh37 chr2: 118,872,395-128,069,813 , GRCh38.p12 chr2: 118,114,819-127,312,237 C2orf76, LOC107985817, 89 more genes
    nsv4519384copy number variation1nstd166human GRCh37.p13 chr2: 119,819,998-124,091,000 , GRCh38.p12 chr2: 119,062,422-123,333,424 LOC105373593, LOC105373596, 54 more genes
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