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Items: 1 to 20 of 546

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148081copy number variation1nstd102humanPathogenic GRCh37 chr3: 10,167,260-12,533,766 , GRCh38.p12 chr3: 10,125,576-12,492,267 SLC6A1-AS1, LOC101927467, 37 more genes
    nsv7057436inversion1nstd229human GRCh38 chr3: 11,572,735-11,719,973 , GRCh37.p13 chr3: 11,614,209-11,761,447 TAMM41, VGLL4
    nsv7042755inversion1nstd229human GRCh38 chr3: 8,982,205-12,221,239 , GRCh37.p13 chr3: 9,023,889-12,262,739 SYN2, MTCO1P5, 74 more genes
    nsv6715429copy number variation1nstd229human GRCh38 chr3: 11,830,486-11,830,871 , GRCh37.p13 chr3: 11,871,960-11,872,345 TAMM41
    nsv6714054copy number variation1nstd229human GRCh38 chr3: 11,717,164-11,820,353 , GRCh37.p13 chr3: 11,758,638-11,861,827 TAMM41, VGLL4
    nsv6713212copy number variation1nstd229human GRCh38 chr3: 11,737,910-11,743,696 , GRCh37.p13 chr3: 11,779,384-11,785,170 TAMM41
    nsv6711347copy number variation1nstd229human GRCh38 chr3: 11,840,264-11,879,924 , GRCh37.p13 chr3: 11,881,738-11,921,398 TAMM41, CYCSP12, 1 more genes
    nsv6711219copy number variation1nstd229human GRCh38 chr3: 11,626,401-11,828,000 , GRCh37.p13 chr3: 11,667,875-11,869,474 TAMM41, VGLL4
    nsv6710832copy number variation1nstd229human GRCh38 chr3: 11,722,412-11,841,696 , GRCh37.p13 chr3: 11,763,886-11,883,170 TAMM41
    nsv6709479copy number variation1nstd229human GRCh38 chr3: 11,800,976-11,810,414 , GRCh37.p13 chr3: 11,842,450-11,851,888 TAMM41
    nsv6708929copy number variation1nstd229human GRCh38 chr3: 11,796,501-11,798,700 , GRCh37.p13 chr3: 11,837,975-11,840,174 TAMM41
    nsv6708557copy number variation1nstd229human GRCh38 chr3: 11,733,413-11,741,697 , GRCh37.p13 chr3: 11,774,887-11,783,171 TAMM41
    nsv6708033copy number variation1nstd229human GRCh38 chr3: 11,744,881-11,744,963 , GRCh37.p13 chr3: 11,786,355-11,786,437 TAMM41
    nsv6706375copy number variation1nstd229human GRCh38 chr3: 11,681,851-11,720,691 , GRCh37.p13 chr3: 11,723,325-11,762,165 TAMM41, VGLL4
    nsv6705914copy number variation1nstd229human GRCh38 chr3: 11,760,810-11,766,417 , GRCh37.p13 chr3: 11,802,284-11,807,891 TAMM41
    nsv6705228copy number variation1nstd229human GRCh38 chr3: 11,702,053-11,851,666 , GRCh37.p13 chr3: 11,743,527-11,893,140 TAMM41, VGLL4
    nsv6704882copy number variation1nstd229human GRCh38 chr3: 11,696,501-11,870,700 , GRCh37.p13 chr3: 11,737,975-11,912,174 TAMM41, VGLL4, 1 more genes
    nsv6704071copy number variation1nstd229human GRCh38 chr3: 11,795,081-11,795,291 , GRCh37.p13 chr3: 11,836,555-11,836,765 TAMM41
    nsv6703249copy number variation1nstd229human GRCh38 chr3: 11,752,756-11,763,231 , GRCh37.p13 chr3: 11,794,230-11,804,705 TAMM41
    nsv6702886copy number variation1nstd229human GRCh38 chr3: 11,754,827-11,755,054 , GRCh37.p13 chr3: 11,796,301-11,796,528 TAMM41
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