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Items: 1 to 20 of 198

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5443249copy number variation1nstd206human GRCh38 chr3: 52,832,609-52,855,972 , GRCh37.p13 chr3: 52,866,625-52,889,988 STIMATE-MUSTN1, MIR8064, 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
    nsv4914349copy number variation1nstd200human GRCh38 chr3: 52,863,403-52,865,788 , GRCh37.p13 chr3: 52,897,419-52,899,804 STIMATE, STIMATE-MUSTN1
    nsv4914348copy number variation1nstd200human GRCh38 chr3: 52,832,609-52,855,972 , GRCh37.p13 chr3: 52,866,625-52,889,988 STIMATE, STIMATE-MUSTN1, 2 more genes
    nsv4911392copy number variation1nstd200human GRCh38 chr3: 52,863,528-52,865,675 , GRCh37.p13 chr3: 52,897,544-52,899,691 STIMATE, STIMATE-MUSTN1
    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
    nsv4793992copy number variation1nstd200human GRCh37 chr3: 52,897,419-52,899,804 , GRCh38.p12 chr3: 52,863,403-52,865,788 STIMATE, STIMATE-MUSTN1
    nsv4793991copy number variation1nstd200human GRCh37 chr3: 52,866,625-52,889,988 , GRCh38.p12 chr3: 52,832,609-52,855,972 STIMATE, STIMATE-MUSTN1, 2 more genes
    nsv4730120inversion1nstd198human GRCh37.p13 chr3: 52,893,520-52,893,550 , GRCh38 chr3: 52,859,504-52,859,534 STIMATE, STIMATE-MUSTN1
    nsv4679783copy number variation1nstd189human GRCh37.p13 chr3: 52,082,781-53,128,685 , GRCh38.p12 chr3: 52,048,765-53,094,669 , ALAS1, 50 more genes
    nsv4673975copy number variation1nstd102humanUncertain significance GRCh37 chr3: 51,247,306-53,069,942 , GRCh38.p12 chr3: 51,209,875-53,035,926 RRP9, LOC100301990, 76 more genes
    nsv4567497mobile element insertion1nstd166human GRCh37.p13 chr3: 52,887,790-52,887,790 , GRCh38.p12 chr3: 52,853,774-52,853,774 STIMATE-MUSTN1, STIMATE
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4453518copy number variation1nstd102humanPathogenic GRCh37 chr3: 52,195,134-52,869,037 , GRCh38.p12 chr3: 52,161,118-52,835,021 SNORD19B, TLR9, 42 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
    nsv4091549copy number variation1nstd166human GRCh37.p13 chr3: 52,912,298-52,913,057 , GRCh38.p12 chr3: 52,878,282-52,879,041 STIMATE, STIMATE-MUSTN1
    nsv4086728copy number variation1nstd166human GRCh37.p13 chr3: 52,866,625-52,889,988 , GRCh38.p12 chr3: 52,832,609-52,855,972 MUSTN1, MIR8064, 2 more genes
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