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Items: 1 to 20 of 90

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5900934copy number variation1nstd209human GRCh38 chr3: 39,322,458-39,330,832 , GRCh37.p13 chr3: 39,363,949-39,372,323 CCR8
    nsv5900268copy number variation1nstd209human GRCh38 chr3: 39,310,860-39,368,788 , GRCh37.p13 chr3: 39,352,351-39,410,279 CCR8, HNRNPA1P21, 2 more genes
    nsv5835943copy number variation1nstd209human GRCh38 chr3: 39,321,954-39,330,802 , GRCh37.p13 chr3: 39,363,445-39,372,293 CCR8
    nsv5441673copy number variation1nstd206human GRCh38 chr3: 39,310,874-39,368,783 , GRCh37.p13 chr3: 39,352,365-39,410,274 EEF1A1P24, CCR8, 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
    nsv4910878copy number variation1nstd200human GRCh38 chr3: 39,310,895-39,368,763 , GRCh37.p13 chr3: 39,352,386-39,410,254 LOC105377644, CCR8, 2 more genes
    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
    nsv4806643copy number variation1nstd200human GRCh37 chr3: 39,352,374-39,410,278 , GRCh38.p12 chr3: 39,310,883-39,368,787 CCR8, EEF1A1P24, 2 more genes
    nsv4777766mobile element deletion1nstd200human GRCh37 chr3: 39,372,946-39,373,257 , GRCh38.p12 chr3: 39,331,455-39,331,766 CCR8
    nsv4586141copy number variation2nstd183human GRCh37 chr3: 39,351,485-39,414,079 , GRCh38.p12 chr3: 39,309,994-39,372,588 EEF1A1P24, HNRNPA1P21, 3 more genes
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4407253copy number variation1nstd174human GRCh37 chr3: 39,351,485-39,414,079 , GRCh38.p12 chr3: 39,309,994-39,372,588 HNRNPA1P21, LOC105377644, 3 more genes
    nsv4377011copy number variation1nstd173human GRCh37 chr3: 39,357,061-39,401,107 , GRCh38.p12 chr3: 39,315,570-39,359,616 HNRNPA1P21, CCR8, 2 more genes
    nsv4371950copy number variation1nstd173human GRCh37 chr3: 39,370,536-39,401,107 , GRCh38.p12 chr3: 39,329,045-39,359,616 CCR8, HNRNPA1P21, 2 more genes
    nsv4080849copy number variation1nstd166human GRCh37.p13 chr3: 39,353,000-39,410,000 , GRCh38.p12 chr3: 39,311,509-39,368,509 LOC105377644, HNRNPA1P21, 2 more genes
    nsv4076899copy number variation1nstd166human GRCh37.p13 chr3: 39,372,529-39,373,287 , GRCh38.p12 chr3: 39,331,038-39,331,796 CCR8
    nsv4076124copy number variation1nstd166human GRCh37.p13 chr3: 39,363,926-39,372,324 , GRCh38.p12 chr3: 39,322,435-39,330,833 CCR8
    nsv4073342copy number variation1nstd166human GRCh37.p13 chr3: 39,367,242-39,406,328 , GRCh38.p12 chr3: 39,325,751-39,364,837 HNRNPA1P21, CCR8, 2 more genes
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