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Items: 1 to 20 of 463

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5949037insertion1nstd209human GRCh38 chr3: 160,237,516-160,237,516 , GRCh37.p13 chr3: 159,955,303-159,955,303 TRIM59-IFT80
    nsv5907302copy number variation1nstd209human GRCh38 chr3: 160,480,396-160,481,131 , GRCh37.p13 chr3: 160,198,184-160,198,919 TRIM59-IFT80
    nsv5904237copy number variation1nstd209human GRCh38 chr3: 160,366,442-160,366,511 , GRCh37.p13 chr3: 160,084,230-160,084,299 TRIM59-IFT80, IFT80
    nsv5901508copy number variation1nstd209human GRCh38 chr3: 160,326,312-160,326,474 , GRCh37.p13 chr3: 160,044,100-160,044,262 IFT80, TRIM59-IFT80
    nsv5900719copy number variation1nstd209human GRCh38 chr3: 160,408,999-160,409,289 , GRCh37.p13 chr3: 160,126,787-160,127,077 SMC4, TRIM59-IFT80
    nsv5900688copy number variation1nstd209human GRCh38 chr3: 160,379,464-160,382,477 , GRCh37.p13 chr3: 160,097,252-160,100,265 IFT80, TRIM59-IFT80
    nsv5897472copy number variation1nstd209human GRCh38 chr3: 160,426,572-160,426,678 , GRCh37.p13 chr3: 160,144,360-160,144,466 TRIM59-IFT80, SMC4
    nsv5896270copy number variation1nstd209human GRCh38 chr3: 160,435,429-160,439,577 , GRCh37.p13 chr3: 160,153,217-160,157,365 TRIM59, SMC4, 1 more genes
    nsv5835020copy number variation1nstd209human GRCh38 chr3: 160,435,394-160,439,293 , GRCh37.p13 chr3: 160,153,182-160,157,081 SMC4, TRIM59, 1 more genes
    nsv5835019copy number variation1nstd209human GRCh38 chr3: 160,381,293-160,382,492 , GRCh37.p13 chr3: 160,099,081-160,100,280 IFT80, TRIM59-IFT80
    nsv5725071mobile element insertion1nstd211human GRCh38 chr3: 160,328,483-160,328,483 , GRCh37.p13 chr3: 160,046,271-160,046,271 TRIM59-IFT80, IFT80
    nsv5722953mobile element insertion1nstd211human GRCh38 chr3: 160,251,334-160,251,334 , GRCh37.p13 chr3: 159,969,121-159,969,121 TRIM59-IFT80
    nsv5716141mobile element insertion1nstd211human GRCh38 chr3: 160,390,431-160,390,431 , GRCh37.p13 chr3: 160,108,219-160,108,219 IFT80, TRIM59-IFT80
    nsv5685164mobile element insertion2nstd211human GRCh38 chr3: 160,299,251-160,299,251 , GRCh37.p13 chr3: 160,017,039-160,017,039 TRIM59-IFT80, IFT80
    nsv5682121mobile element insertion1nstd211human GRCh38 chr3: 160,467,262-160,467,262 , GRCh37.p13 chr3: 160,185,050-160,185,050 TRIM59-IFT80
    nsv5680431mobile element insertion1nstd211human GRCh38 chr3: 160,283,020-160,283,020 , GRCh37.p13 chr3: 160,000,808-160,000,808 IFT80, TRIM59-IFT80
    nsv5674902mobile element insertion1nstd211human GRCh38 chr3: 160,312,925-160,312,925 , GRCh37.p13 chr3: 160,030,713-160,030,713 TRIM59-IFT80, IFT80
    nsv5610955insertion1nstd207human GRCh38 chr3: 160,409,111-160,409,111 , GRCh37.p13 chr3: 160,126,899-160,126,899 TRIM59-IFT80, SMC4
    nsv5610226insertion1nstd207human GRCh38 chr3: 160,312,973-160,312,973 , GRCh37.p13 chr3: 160,030,761-160,030,761 TRIM59-IFT80, IFT80
    nsv5564435copy number variation1nstd102humanUncertain significance GRCh37 chr3: 160,075,257-160,075,386 , GRCh38.p12 chr3: 160,357,469-160,357,598 IFT80, TRIM59-IFT80
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