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Items: 1 to 20 of 211

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093619copy number variation1nstd228human GRCh37 chr4: 171,508,974-190,957,473 , GRCh38.p12 chr4: 170,587,823-190,036,318 AGA, SLC25A4, 240 more genes
    nsv7056217inversion1nstd229human GRCh38 chr4: 166,607,935-172,500,612 , GRCh37.p13 chr4: 167,529,086-173,421,763 DDX60, LOC105377529, 50 more genes
    nsv7054944inversion1nstd229human GRCh38 chr4: 169,647,111-171,933,053 , GRCh37.p13 chr4: 170,568,262-172,854,204 PTGES3P3, LOC402192, 23 more genes
    nsv7038664inversion1nstd229human GRCh38 chr4: 170,091,988-172,217,645 , GRCh37.p13 chr4: 171,013,139-173,138,796 MIR6082, LINC02504, 14 more genes
    nsv6757861copy number variation1nstd229human GRCh38 chr4: 170,744,632-172,189,564 , GRCh37.p13 chr4: 171,665,783-173,110,715 LINC02504, MIR6082, 8 more genes
    nsv6757355copy number variation1nstd229human GRCh38 chr4: 171,278,954-171,287,897 , GRCh37.p13 chr4: 172,200,105-172,209,048 LOC105377534, LINC02504
    nsv6757081copy number variation1nstd229human GRCh38 chr4: 171,081,875-171,364,198 , GRCh37.p13 chr4: 172,003,026-172,285,349 LOC101929135, LOC105377534, 2 more genes
    nsv6753889copy number variation1nstd229human GRCh38 chr4: 171,285,921-171,323,045 , GRCh37.p13 chr4: 172,207,072-172,244,196 LINC02504, LOC105377534
    nsv6753217copy number variation1nstd229human GRCh38 chr4: 170,394,754-173,096,756 , GRCh37.p13 chr4: 171,315,905-174,017,907 HSP90AA6P, MIR6082, 14 more genes
    nsv6750773copy number variation1nstd229human GRCh38 chr4: 171,237,501-171,371,700 , GRCh37.p13 chr4: 172,158,652-172,292,851 LINC02504, LOC105377534
    nsv6748748copy number variation1nstd229human GRCh38 chr4: 170,291,461-171,359,315 , GRCh37.p13 chr4: 171,212,612-172,280,466 LINC02431, LOC101929135, 7 more genes
    nsv6746712copy number variation1nstd229human GRCh38 chr4: 171,237,542-171,371,657 , GRCh37.p13 chr4: 172,158,693-172,292,808 LOC105377534, LINC02504
    nsv6743801copy number variation1nstd229human GRCh38 chr4: 171,235,920-171,288,512 , GRCh37.p13 chr4: 172,157,071-172,209,663 LINC02504, LOC105377534
    nsv6634364copy number variation1nstd102humanPathogenic GRCh37 chr4: 167,779,888-190,957,473 , GRCh38.p12 chr4: 166,858,737-190,036,318 LOC101928551, LOC107986330, 279 more genes
    nsv6634351copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,174,483-190,957,473 , GRCh38.p12 chr4: 158,253,331-190,036,318 COPS3P1, LOC339975, 363 more genes
    nsv6570050inversion1nstd223human GRCh38 chr4: 169,780,525-178,315,900 , GRCh37.p13 chr4: 170,701,676-179,237,054 LOC101928409, LOC100131553, 91 more genes
    nsv6392123copy number variation1nstd223human GRCh38 chr4: 171,273,842-171,439,274 , GRCh37.p13 chr4: 172,194,993-172,360,425 LOC105377534, LINC02504
    nsv6390736copy number variation1nstd223human GRCh38 chr4: 171,286,501-171,288,100 , GRCh37.p13 chr4: 172,207,652-172,209,251 LOC105377534, LINC02504
    nsv6390028copy number variation1nstd223human GRCh38 chr4: 171,285,920-171,323,043 , GRCh37.p13 chr4: 172,207,071-172,244,194 LINC02504, LOC105377534
    nsv6377842copy number variation1nstd223human GRCh38 chr4: 168,709,595-174,342,624 , GRCh37.p13 chr4: 169,630,746-175,263,775 LOC105377527, LOC107986203, 64 more genes
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