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Items: 1 to 20 of 135

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5888903copy number variation1nstd209human GRCh38 chr3: 97,972,383-97,972,456 , GRCh37.p13 chr3: 97,691,227-97,691,300 RIOX2
    nsv5557351sequence alteration1nstd206human GRCh38 chr3: 97,956,692-97,957,555 , GRCh37.p13 chr3: 97,675,536-97,676,399 RIOX2
    nsv5539192insertion1nstd206human GRCh38 chr3: 97,956,730-97,956,730 , GRCh37.p13 chr3: 97,675,574-97,675,574 RIOX2
    nsv5452260copy number variation1nstd206human GRCh38 chr3: 97,954,609-97,954,693 , GRCh37.p13 chr3: 97,673,453-97,673,537 RIOX2
    nsv5377488translocation1nstd200human GRCh38 chr3: 46,702,651-46,702,651 , GRCh38 chr3: 97,960,281-97,960,281 , GRCh37.p13 chr3: 46,744,141-46,744,141 , GRCh37.p13 chr3: 97,679,125-97,679,125 RIOX2, TMIE
    nsv5316670copy number variation1nstd204human GRCh38.p13 chr3: 97,709,287-98,121,663 , GRCh37.p13 chr3: 97,428,131-97,840,507 LOC105373994, ARL6, 10 more genes
    nsv5234199copy number variation1nstd204human GRCh38.p13 chr3: 97,708,701-98,121,600 , GRCh37.p13 chr3: 97,427,545-97,840,444 LOC105373994, ARL6, 10 more genes
    nsv5224437copy number variation1nstd204human GRCh38.p13 chr3: 97,970,168-97,991,379 , GRCh37.p13 chr3: 97,689,012-97,710,223 GABRR3, RIOX2
    nsv5085324mobile element insertion1nstd203human GRCh38 chr3: 97,972,611-97,972,646 , GRCh37.p13 chr3: 97,691,455-97,691,490 RIOX2
    nsv5084060mobile element insertion1nstd203human GRCh38 chr3: 97,955,207-97,955,224 , GRCh37.p13 chr3: 97,674,051-97,674,068 RIOX2
    nsv5040665inversion1nstd200human GRCh38 chr3: 94,638,746-100,409,115 , GRCh37.p13 chr3: 94,357,590-100,127,959 , LOC101929278, 82 more genes
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5034224inversion1nstd200human GRCh38 chr3: 94,859,289-102,665,887 , GRCh37.p13 chr3: 94,578,133-102,384,731 , LOC105374005, 114 more genes
    nsv4919066copy number variation1nstd200human GRCh38 chr3: 97,958,994-97,967,284 , GRCh37.p13 chr3: 97,677,838-97,686,128 RIOX2
    nsv4919065copy number variation1nstd200human GRCh38 chr3: 97,955,196-97,956,590 , GRCh37.p13 chr3: 97,674,040-97,675,434 RIOX2
    nsv4919064copy number variation1nstd200human GRCh38 chr3: 97,954,609-97,954,693 , GRCh37.p13 chr3: 97,673,453-97,673,537 RIOX2
    nsv4919060copy number variation1nstd200human GRCh38 chr3: 97,824,265-98,358,535 , GRCh37.p13 chr3: 97,543,109-98,077,379 OR5AC2, OR5H8, 23 more genes
    nsv4887622inversion1nstd200human GRCh37 chr3: 94,357,590-100,127,961 , GRCh38.p12 chr3: 94,638,746-100,409,117 , CPOX, 82 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4797621copy number variation1nstd200human GRCh37 chr3: 97,674,039-97,675,435 , GRCh38.p12 chr3: 97,955,195-97,956,591 RIOX2
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