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Items: 1 to 20 of 122

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5888582copy number variation1nstd209human GRCh38 chr3: 46,802,705-48,210,414 , GRCh37.p13 chr3: 46,844,195-48,251,904 SNORD13P3, LOC105377074, 34 more genes
    nsv5836340copy number variation1nstd209human GRCh38 chr3: 47,559,865-47,561,114 , GRCh37.p13 chr3: 47,601,355-47,602,604 CSPG5, RN7SL870P
    nsv5836305copy number variation1nstd209human GRCh38 chr3: 47,567,615-47,577,835 , GRCh37.p13 chr3: 47,609,105-47,619,325 CSPG5
    nsv5836304copy number variation1nstd209human GRCh38 chr3: 47,532,860-47,568,954 , GRCh37.p13 chr3: 47,574,350-47,610,444 LOC105377074, RN7SL870P, 1 more genes
    nsv5716957mobile element insertion1nstd211human GRCh38 chr3: 47,561,608-47,561,608 , GRCh37.p13 chr3: 47,603,098-47,603,098 CSPG5
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5557815mobile element insertion1nstd206human GRCh38 chr3: 47,561,608-47,561,659 , GRCh37.p13 chr3: 47,603,098-47,603,149 CSPG5
    nsv5439202copy number variation1nstd206human GRCh38 chr3: 47,559,907-47,561,107 , GRCh37.p13 chr3: 47,601,397-47,602,597 CSPG5, RN7SL870P
    nsv5214341mobile element deletion1nstd204human GRCh38.p13 chr3: 47,576,428-47,576,783 , GRCh37.p13 chr3: 47,617,918-47,618,273 CSPG5
    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
    nsv4924397copy number variation1nstd200human GRCh38 chr3: 47,344,940-47,923,420 , GRCh37.p13 chr3: 47,386,430-47,964,910 PTPN23, DHX30, 13 more genes
    nsv4911162copy number variation1nstd200human GRCh38 chr3: 47,579,328-47,579,399 , GRCh37.p13 chr3: 47,620,818-47,620,889 CSPG5
    nsv4911161copy number variation1nstd200human GRCh38 chr3: 47,569,772-47,570,771 , GRCh37.p13 chr3: 47,611,262-47,612,261 CSPG5
    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
    nsv4806731copy number variation1nstd200human GRCh37 chr3: 47,620,818-47,620,889 , GRCh38.p12 chr3: 47,579,328-47,579,399 CSPG5
    nsv4777782mobile element deletion1nstd200human GRCh37 chr3: 47,617,943-47,618,249 , GRCh38.p12 chr3: 47,576,453-47,576,759 CSPG5
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4347762copy number variation1nstd102humanPathogenic GRCh37 chr3: 45,153,770-53,878,616 , GRCh38.p12 chr3: 45,112,278-53,844,589 UQCRC1, DHX30, 291 more genes
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