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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5873481copy number variation1nstd209human GRCh38 chr1: 153,419,111-153,428,488 , GRCh37.p13 chr1: 153,391,587-153,400,964 S100A8, S100A7P1, 1 more genes
    nsv5828145copy number variation1nstd209human GRCh38 chr1: 153,419,076-153,421,410 , GRCh37.p13 chr1: 153,391,552-153,393,886 S100A8, S100A7A
    nsv5724675mobile element insertion1nstd211human GRCh38 chr1: 153,409,165-153,409,165 , GRCh37.p13 chr1: 153,381,641-153,381,641 S100A8
    nsv5563935sequence alteration1nstd206human GRCh38 chr1: 153,417,880-153,459,217 , GRCh37.p13 chr1: 153,390,356-153,431,693 S100A7, S100A8, 4 more genes
    nsv5556873inversion1nstd206human GRCh38 chr1: 153,417,393-153,459,649 , GRCh37.p13 chr1: 153,389,869-153,432,125 S100A7, S100A8, 4 more genes
    nsv5426212copy number variation1nstd206human GRCh38 chr1: 153,399,399-153,399,819 , GRCh37.p13 chr1: 153,371,875-153,372,295 S100A8
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5370709translocation1nstd200human GRCh38 chr1: 153,463,206-153,463,206 , GRCh38 chr1: 153,413,788-153,413,788 , GRCh37.p13 chr1: 153,435,682-153,435,682 , GRCh37.p13 chr1: 153,386,264-153,386,264 S100A8
    nsv5370706translocation1nstd200human GRCh38 chr1: 153,464,046-153,464,046 , GRCh38 chr1: 153,406,900-153,406,900 , GRCh37.p13 chr1: 153,379,376-153,379,376 , GRCh37.p13 chr1: 153,436,522-153,436,522 S100A8
    nsv5331063translocation1nstd200human GRCh37 chr1: 153,431,452-153,431,452 , GRCh37 chr1: 153,390,590-153,390,590 , GRCh38.p12 chr1: 153,418,114-153,418,114 , GRCh38.p12 chr1: 153,458,976-153,458,976 S100A7, S100A8, 1 more genes
    nsv4903888copy number variation1nstd200human GRCh38 chr1: 153,340,507-153,523,038 , GRCh37.p13 chr1: 153,312,983-153,495,514 S100A8, S100A7P1, 10 more genes
    nsv4897450copy number variation1nstd200human GRCh38 chr1: 153,418,888-153,419,652 , GRCh37.p13 chr1: 153,391,364-153,392,128 S100A7A, S100A8
    nsv4897449copy number variation1nstd200human GRCh38 chr1: 153,405,188-153,407,741 , GRCh37.p13 chr1: 153,377,664-153,380,217 S100A8
    nsv4784246copy number variation1nstd200human GRCh37 chr1: 153,371,875-153,372,295 , GRCh38.p12 chr1: 153,399,399-153,399,819 S100A8
    nsv4781202copy number variation1nstd200human GRCh37 chr1: 153,312,983-153,495,514 , GRCh38.p12 chr1: 153,340,507-153,523,038 S100A9, S100A12, 10 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4728602copy number variation1nstd102humanUncertain significance GRCh37 chr1: 153,007,105-153,463,223 , GRCh38.p12 chr1: 153,034,629-153,490,747 S100A8, S100A7P1, 23 more genes
    nsv4716344copy number variation1nstd195human GRCh38.p12 chr1: 153,319,675-153,409,725 , GRCh37 chr1: 153,292,151-153,382,201 S100A8, S100A9, 5 more genes
    nsv4708254copy number variation1nstd195human GRCh37 chr1: 153,385,351-153,414,501 , GRCh38.p12 chr1: 153,412,875-153,442,025 S100A8, S100A7P1, 2 more genes
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