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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5899856copy number variation1nstd209human GRCh38 chr3: 12,869,127-12,876,213 , GRCh37.p13 chr3: 12,910,626-12,917,712 LOC105376956, LINC02022
    nsv5071193mobile element insertion1nstd203human GRCh38 chr3: 12,881,927-12,881,950 , GRCh37.p13 chr3: 12,923,426-12,923,449 LINC02022, LOC105376956
    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
    nsv4924190copy number variation1nstd200human GRCh38 chr3: 12,867,496-12,974,461 , GRCh37.p13 chr3: 12,908,995-13,015,961 LINC02022, LOC105376956, 1 more genes
    nsv4917855copy number variation1nstd200human GRCh38 chr3: 12,868,787-12,876,198 , GRCh37.p13 chr3: 12,910,286-12,917,697 LOC105376956, LINC02022
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4796371copy number variation1nstd200human GRCh37 chr3: 12,910,622-12,917,764 , GRCh38.p12 chr3: 12,869,123-12,876,265 LINC02022, LOC105376956
    nsv4796370copy number variation1nstd200human GRCh37 chr3: 12,910,315-12,917,358 , GRCh38.p12 chr3: 12,868,816-12,875,859 LOC105376956, LINC02022
    nsv4793852copy number variation1nstd200human GRCh37 chr3: 12,908,995-13,015,961 , GRCh38.p12 chr3: 12,867,496-12,974,461 LOC105376956, IQSEC1, 1 more genes
    nsv4572522sequence alteration1nstd166human GRCh37.p13 chr3: 12,914,421-12,925,342 , GRCh38.p12 chr3: 12,872,922-12,883,843 LINC02022, LOC105376956
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4088256copy number variation1nstd166human GRCh37.p13 chr3: 12,914,052-12,933,148 , GRCh38.p12 chr3: 12,872,553-12,891,649 LINC02022, LOC105376956
    nsv4086094copy number variation1nstd166human GRCh37.p13 chr3: 12,919,963-12,923,259 , GRCh38.p12 chr3: 12,878,464-12,881,760 LINC02022, LOC105376956
    nsv4079758copy number variation1nstd166human GRCh37.p13 chr3: 12,922,589-12,922,716 , GRCh38.p12 chr3: 12,881,090-12,881,217 LOC105376956, LINC02022
    nsv4078030copy number variation1nstd166human GRCh37.p13 chr3: 12,920,170-12,922,404 , GRCh38.p12 chr3: 12,878,671-12,880,905 LINC02022, LOC105376956
    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
    nsv3917079copy number variation1nstd102humanUncertain significance NCBI36 chr3: 12,504,064-13,013,825 , GRCh37 chr3: 12,529,064-13,038,825 , GRCh38 chr3: 12,487,565-12,997,325 RNU6-377P, CAND2, 16 more genes
    nsv3907461copy number variation1nstd102humanPathogenic GRCh38 chr3: 63,843-19,510,600 , GRCh37 chr3: 105,526-19,552,092 , NCBI36 chr3: 80,526-19,527,096 TAMM41, CYCSP11, 267 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
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