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Items: 1 to 20 of 258

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5638072insertion1nstd207human GRCh38 chr6: 170,255,981-170,255,981 , GRCh37.p13 chr6: 170,565,069-170,565,069 LOC154449
    nsv5628959insertion1nstd207human GRCh38 chr6: 170,253,285-170,253,285 , GRCh37.p13 chr6: 170,562,373-170,562,373 LOC154449
    nsv5583573copy number variation1nstd207human GRCh38 chr6: 170,253,280-170,253,329 , GRCh37.p13 chr6: 170,562,368-170,562,417 LOC154449
    nsv5569485copy number variation1nstd207human GRCh38 chr6: 170,255,827-170,255,895 , GRCh37.p13 chr6: 170,564,915-170,564,983 LOC154449
    nsv5454459copy number variation1nstd206human GRCh38 chr6: 170,255,455-170,258,783 , GRCh37.p13 chr6: 170,564,543-170,567,871 LOC154449
    nsv5370069translocation1nstd200human GRCh38 chr6: 170,255,455-170,255,455 , GRCh38 chr6: 170,258,783-170,258,783 , GRCh37.p13 chr6: 170,564,543-170,564,543 , GRCh37.p13 chr6: 170,567,871-170,567,871 LOC154449
    nsv5342295translocation1nstd200human GRCh37 chr6: 170,567,871-170,567,871 , GRCh37 chr6: 170,564,543-170,564,543 , GRCh38.p12 chr6: 170,255,455-170,255,455 , GRCh38.p12 chr6: 170,258,783-170,258,783 LOC154449
    nsv5307218copy number variation1nstd204human GRCh38.p13 chr6: 170,255,452-170,258,791 , GRCh37.p13 chr6: 170,564,540-170,567,879 LOC154449
    nsv5305606copy number variation1nstd204human GRCh38.p13 chr6: 170,056,994-170,362,978 , GRCh37.p13 chr6: 170,372,218-170,672,066 MIR4644, LINC01624, 8 more genes
    nsv5232939copy number variation1nstd204human GRCh38.p13 chr6: 170,255,511-170,258,916 , GRCh37.p13 chr6: 170,564,599-170,568,004 LOC154449
    nsv5220488copy number variation1nstd204human GRCh37.p13 chr6: 170,547,089-170,672,088 , GRCh38.p13 chr6: 170,238,001-170,363,000 DLL1, FAM120B, 4 more genes
    nsv4966084copy number variation1nstd200human GRCh38 chr6: 170,251,111-170,252,691 , GRCh37.p13 chr6: 170,560,199-170,561,779 LOC154449
    nsv4966083copy number variation1nstd200human GRCh38 chr6: 170,248,428-170,254,528 , GRCh37.p13 chr6: 170,557,516-170,563,616 LOC154449
    nsv4953156copy number variation1nstd200human GRCh38 chr6: 170,247,250-170,272,698 , GRCh37.p13 chr6: 170,556,338-170,581,786 LINC01624, LOC285804, 1 more genes
    nsv4824924copy number variation1nstd200human GRCh37 chr6: 170,372,228-170,672,064 , GRCh38.p12 chr6: 170,057,004-170,362,976 RPL12P23, LOC285804, 8 more genes
    nsv4818164copy number variation1nstd200human GRCh37 chr6: 170,560,199-170,561,779 , GRCh38.p12 chr6: 170,251,111-170,252,691 LOC154449
    nsv4738326copy number variation1nstd199human GRCh37 chr6: 170,562,391-170,562,445 , GRCh38.p12 chr6: 170,253,303-170,253,357 LOC154449
    nsv4734055copy number variation1nstd199human GRCh37 chr6: 170,564,943-170,565,012 , GRCh38.p12 chr6: 170,255,855-170,255,924 LOC154449
    nsv4729645copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 166,083,476-170,919,482 , GRCh38.p12 chr6: 165,669,988-170,610,394 CCR6, GNG5P1, 118 more genes
    nsv4729261copy number variation1nstd102humanPathogenic GRCh37 chr6: 167,580,012-170,919,482 , GRCh38.p12 chr6: 167,166,524-170,610,394 LOC107986549, AFDN, 81 more genes
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