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Items: 1 to 20 of 229

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112673copy number variation1nstd102humanPathogenic GRCh37 chr2: 88,007,281-90,260,248 , GRCh38.p12 chr2: 87,707,762-90,221,382 IGKV3-20, IGKV3-7, 122 more genes
    nsv5882908copy number variation1nstd209human GRCh38 chr2: 88,315,331-88,598,001 , GRCh37.p13 chr2: 88,614,850-88,897,519 EIF2AK3, SPMIP9, 6 more genes
    nsv5874555copy number variation1nstd209human GRCh38 chr2: 88,557,975-88,558,055 , GRCh37.p13 chr2: 88,857,493-88,857,573 EIF2AK3, LOC101928371
    nsv5833850copy number variation1nstd209human GRCh38 chr2: 88,623,287-88,624,386 , GRCh37.p13 chr2: 88,922,805-88,923,904 EIF2AK3
    nsv5833849copy number variation1nstd209human GRCh38 chr2: 88,605,857-88,606,884 , GRCh37.p13 chr2: 88,905,375-88,906,402 EIF2AK3
    nsv5833848copy number variation1nstd209human GRCh38 chr2: 88,588,164-88,597,570 , GRCh37.p13 chr2: 88,887,682-88,897,088 EIF2AK3
    nsv5833847copy number variation1nstd209human GRCh38 chr2: 88,587,121-88,589,363 , GRCh37.p13 chr2: 88,886,639-88,888,881 EIF2AK3
    nsv5833846copy number variation2nstd209human GRCh38 chr2: 88,579,550-88,585,213 , GRCh37.p13 chr2: 88,879,068-88,884,731 EIF2AK3
    nsv5833489copy number variation1nstd209human GRCh38 chr2: 88,535,873-88,572,558 , GRCh37.p13 chr2: 88,835,391-88,872,076 LOC101928371, EIF2AK3
    nsv5686869mobile element insertion1nstd211human GRCh38 chr2: 88,627,844-88,627,844 , GRCh37.p13 chr2: 88,927,362-88,927,362 EIF2AK3, EIF2AK3-DT
    nsv5674698mobile element insertion2nstd211human GRCh38 chr2: 88,576,479-88,576,479 , GRCh37.p13 chr2: 88,875,997-88,875,997 EIF2AK3
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5436982copy number variation1nstd206human GRCh38 chr2: 85,539,948-89,142,574 , GRCh37.p13 chr2: 85,767,071-89,442,057 , IGKV2-18, 129 more genes
    nsv5402911mobile element insertion1nstd206human GRCh38 chr2: 88,627,844-88,627,895 , GRCh37.p13 chr2: 88,927,362-88,927,413 EIF2AK3-DT, EIF2AK3
    nsv5394817mobile element insertion1nstd206human GRCh38 chr2: 88,576,479-88,576,530 , GRCh37.p13 chr2: 88,875,997-88,876,048 EIF2AK3
    nsv5066629mobile element insertion1nstd203human GRCh38 chr2: 88,607,434-88,607,450 , GRCh37.p13 chr2: 88,906,952-88,906,968 EIF2AK3
    nsv5062837mobile element insertion1nstd203human GRCh38 chr2: 88,576,463-88,576,479 , GRCh37.p13 chr2: 88,875,981-88,875,997 EIF2AK3
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4902453copy number variation1nstd200human GRCh38 chr2: 88,559,839-88,560,103 , GRCh37.p13 chr2: 88,859,357-88,859,621 LOC101928371, EIF2AK3
    nsv4776955copy number variation1nstd200human GRCh37 chr2: 88,859,357-88,859,621 , GRCh38.p12 chr2: 88,559,839-88,560,103 LOC101928371, EIF2AK3
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