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Items: 1 to 20 of 216

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5955505insertion1nstd209human GRCh38 chr3: 9,809,959-9,809,959 , GRCh37.p13 chr3: 9,851,643-9,851,643 TTLL3, ARPC4-TTLL3
    nsv5906650copy number variation1nstd209human GRCh38 chr3: 9,795,842-9,796,687 , GRCh37.p13 chr3: 9,837,526-9,838,371 ARPC4, ARPC4-TTLL3
    nsv5894399copy number variation1nstd209human GRCh38 chr3: 9,822,721-9,822,778 , GRCh37.p13 chr3: 9,864,405-9,864,462 TTLL3, ARPC4-TTLL3
    nsv5837521copy number variation1nstd209human GRCh38 chr3: 9,795,715-9,796,714 , GRCh37.p13 chr3: 9,837,399-9,838,398 ARPC4-TTLL3, ARPC4
    nsv5836922copy number variation1nstd209human GRCh38 chr3: 9,824,894-9,829,755 , GRCh37.p13 chr3: 9,866,578-9,871,439 TTLL3, ARPC4-TTLL3
    nsv5682933mobile element insertion1nstd211human GRCh38 chr3: 9,823,498-9,823,498 , GRCh37.p13 chr3: 9,865,182-9,865,182 TTLL3, ARPC4-TTLL3
    nsv5610578insertion1nstd207human GRCh38 chr3: 9,822,721-9,822,721 , GRCh37.p13 chr3: 9,864,405-9,864,405 TTLL3, ARPC4-TTLL3
    nsv5582311copy number variation1nstd207human GRCh38 chr3: 9,836,749-9,837,009 , GRCh37.p13 chr3: 9,878,433-9,878,693 TTLL3, RPUSD3, 1 more genes
    nsv5560704sequence alteration1nstd206human GRCh37.p13 chr3: 9,807,275-9,924,747 , GRCh38 chr3: 9,765,591-9,883,063 OGG1, CAMK1, 7 more genes
    nsv5444197copy number variation1nstd206human GRCh38 chr3: 9,822,729-9,822,804 , GRCh37.p13 chr3: 9,864,413-9,864,488 TTLL3, ARPC4-TTLL3
    nsv5443224copy number variation1nstd206human GRCh38 chr3: 9,800,549-9,800,706 , GRCh37.p13 chr3: 9,842,233-9,842,390 ARPC4, ARPC4-TTLL3
    nsv5326185translocation1nstd204human GRCh37.p13 chr3: 9,864,413-9,864,413 , GRCh37.p13 chr3: 9,864,463-9,864,463 , GRCh38.p13 chr3: 9,822,779-9,822,779 , GRCh38.p13 chr3: 9,822,729-9,822,729 TTLL3, ARPC4-TTLL3
    nsv5311699copy number variation1nstd204human GRCh38.p13 chr3: 9,776,127-10,149,069 , GRCh37.p13 chr3: 9,817,811-10,190,753 EMC3, CYCSP11, 25 more genes
    nsv5212029copy number variation1nstd204human GRCh38.p13 chr3: 9,776,951-9,806,833 , GRCh37.p13 chr3: 9,818,635-9,848,517 ARPC4-TTLL3, TADA3, 2 more genes
    nsv5205129copy number variation1nstd204human GRCh38.p13 chr3: 9,776,301-10,148,700 , GRCh37.p13 chr3: 9,817,985-10,190,384 JAGN1, TTLL3, 25 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
    nsv4917709copy number variation1nstd200human GRCh38 chr3: 9,833,876-9,836,059 , GRCh37.p13 chr3: 9,875,560-9,877,743 TTLL3, ARPC4-TTLL3, 1 more genes
    nsv4917708copy number variation1nstd200human GRCh38 chr3: 9,822,707-9,824,927 , GRCh37.p13 chr3: 9,864,391-9,866,611 TTLL3, ARPC4-TTLL3
    nsv4914303copy number variation1nstd200human GRCh38 chr3: 9,824,844-9,830,084 , GRCh37.p13 chr3: 9,866,528-9,871,768 ARPC4-TTLL3, TTLL3
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