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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148204copy number variation1nstd102humanPathogenic GRCh38 chr5: 9,999-14,320,000 , GRCh37.p13 chr5: 10,001-14,320,109 LOC105379638, LOC100420683, 185 more genes
    nsv7099279copy number variation1nstd231human GRCh37 chr5: 1,810,638-3,031,002 , GRCh38.p12 chr5: 1,810,524-3,030,888 NDUFS6, IRX4, 12 more genes
    nsv7099278copy number variation1nstd231human GRCh37 chr5: 1,804,766-3,031,002 , GRCh38.p12 chr5: 1,804,652-3,030,888 NDUFS6, IRX4, 12 more genes
    nsv7099277copy number variation2nstd231human GRCh37 chr5: 1,804,766-3,030,981 , GRCh38.p12 chr5: 1,804,652-3,030,867 NDUFS6, IRX4, 12 more genes
    nsv7099276copy number variation1nstd231human GRCh37 chr5: 1,804,766-3,028,812 , GRCh38.p12 chr5: 1,804,652-3,028,698 NDUFS6, IRX4, 12 more genes
    nsv7045223inversion1nstd229human GRCh38 chr5: 2,721,510-7,652,208 , GRCh37.p13 chr5: 2,721,624-7,652,321 LOC105374620, LOC105374634, 60 more genes
    nsv6771620copy number variation1nstd229human GRCh38 chr5: 2,616,116-2,817,820 , GRCh37.p13 chr5: 2,616,230-2,817,934 IRX2-DT, LOC100130748, 2 more genes
    nsv6769791copy number variation1nstd229human GRCh38 chr5: 2,749,401-2,751,300 , GRCh37.p13 chr5: 2,749,515-2,751,414 IRX2-DT, IRX2
    nsv6768841copy number variation1nstd229human GRCh38 chr5: 2,735,201-2,751,400 , GRCh37.p13 chr5: 2,735,315-2,751,514 IRX2, IRX2-DT
    nsv6758649copy number variation1nstd229human GRCh38 chr5: 1,642,551-2,905,290 , GRCh37.p13 chr5: 1,642,666-2,905,404 LOC105374618, LOC100506858, 13 more genes
    nsv6758484copy number variation1nstd229human GRCh38 chr5: 2,754,501-2,757,000 , GRCh37.p13 chr5: 2,754,615-2,757,114 IRX2-DT
    nsv6636942copy number variation1nstd102humanPathogenic GRCh37 chr5: 1-32,091,038 , GRCh38.p12 chr5: 10,001-32,090,932 LOC105374608, LSP1P3, 351 more genes
    nsv6636849copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-17,654,787 , GRCh38.p12 chr5: 113,462-17,654,678 ADCY2, HMGB3P3, 248 more genes
    nsv6636672copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-26,164,852 , GRCh38.p12 chr5: 113,462-26,164,743 LINC02123, LINC01020, 302 more genes
    nsv6636606copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-31,448,527 , GRCh38.p12 chr5: 113,462-31,448,420 BASP1, RNU1-76P, 338 more genes
    nsv6574354inversion1nstd223human GRCh38 chr5: 2,721,509-7,652,209 , GRCh37.p13 chr5: 2,721,623-7,652,322 MIR4278, LOC442132, 60 more genes
    nsv6380144copy number variation1nstd223human GRCh38 chr5: 2,755,001-2,755,500 , GRCh37.p13 chr5: 2,755,115-2,755,614 IRX2-DT
    nsv6315441copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-29,310,520 , GRCh38.p12 chr5: 113,461-29,310,413 FBXL7, LOC105374608, 319 more genes
    nsv6315416copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-30,712,376 , GRCh38.p12 chr5: 113,461-30,712,269 LOC105374649, LINC02196, 333 more genes
    nsv6315382copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-8,007,018 , GRCh38.p12 chr5: 113,461-8,006,905 MTCO1P31, LOC100130063, 126 more genes
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