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Items: 1 to 20 of 74

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5902657copy number variation1nstd209human GRCh38 chr3: 25,721,609-25,813,972 , GRCh37.p13 chr3: 25,763,100-25,855,463 OXSM, NGLY1, 2 more genes
    nsv5673477copy number variation1nstd102humanPathogenic GRCh37 chr3: 25,760,931-25,831,376 , GRCh38.p12 chr3: 25,719,440-25,789,885 TAF9BP1, NGLY1, 2 more genes
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4918329copy number variation1nstd200human GRCh38 chr3: 25,767,077-25,816,939 , GRCh37.p13 chr3: 25,808,568-25,858,430 OXSM, NGLY1
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4796720copy number variation1nstd200human GRCh37 chr3: 25,808,568-25,858,430 , GRCh38.p12 chr3: 25,767,077-25,816,939 OXSM, NGLY1
    nsv4586043copy number variation1nstd183human GRCh37 chr3: 25,824,503-25,832,375 , GRCh38.p12 chr3: 25,783,012-25,790,884 OXSM, NGLY1
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4454175copy number variation1nstd102humanUncertain significance GRCh37 chr3: 25,791,210-25,889,888 , GRCh38.p12 chr3: 25,749,719-25,848,397 NGLY1, LOC105377000, 3 more genes
    nsv4452346copy number variation1nstd102humanPathogenic GRCh37 chr3: 19,064,852-26,448,689 , GRCh38.p12 chr3: 19,023,360-26,407,198 RPL15, SGO1, 71 more genes
    nsv4082821copy number variation1nstd166human GRCh37.p13 chr3: 25,820,004-25,837,020 , GRCh38.p12 chr3: 25,778,513-25,795,529 OXSM, NGLY1
    nsv4082272copy number variation1nstd166human GRCh37.p13 chr3: 25,777,117-25,919,314 , GRCh38.p12 chr3: 25,735,626-25,877,823 OXSM, NGLY1, 4 more genes
    nsv3967868copy number variation1nstd168human GRCh38 chr3: 25,781,986-25,823,204 , GRCh37.p13 chr3: 25,823,477-25,864,695 OXSM, NGLY1
    nsv3923656copy number variation1nstd102humanPathogenic GRCh38 chr3: 11,463,328-38,919,543 , NCBI36 chr3: 11,479,802-38,936,038 , GRCh37 chr3: 11,504,802-38,961,034 RN7SL4P, TOP2B, 348 more genes
    nsv3905127copy number variation1nstd102humanPathogenic GRCh37 chr3: 94,991-41,423,012 , NCBI36 chr3: 69,991-41,398,016 , GRCh38 chr3: 53,308-41,381,521 LINC02022, RPL23AP43, 540 more genes
    nsv3901059copy number variation1nstd102humanPathogenic GRCh37 chr3: 73,914-30,105,699 , GRCh38 chr3: 32,241-30,064,208 , NCBI36 chr3: 48,914-30,080,703 RPL32, RPL15, 369 more genes
    nsv3892895copy number variation1nstd102humanPathogenic GRCh38 chr3: 52,266-37,148,076 , GRCh37 chr3: 93,949-37,189,567 , NCBI36 chr3: 68,949-37,164,571 RPL34P11, RNU1-96P, 452 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
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