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Items: 1 to 20 of 219

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv6736779copy number variation1nstd229human GRCh38 chr4: 51,879,262-51,879,787 , GRCh37.p13 chr4: 52,745,428-52,745,953 DCUN1D4
    nsv6735268copy number variation1nstd229human GRCh38 chr4: 51,853,801-51,856,600 , GRCh37.p13 chr4: 52,719,967-52,722,766 DCUN1D4
    nsv6734964copy number variation1nstd229human GRCh38 chr4: 51,893,027-51,893,234 , GRCh37.p13 chr4: 52,759,193-52,759,400 DCUN1D4
    nsv6727926copy number variation1nstd229human GRCh38 chr4: 51,906,099-51,913,334 , GRCh37.p13 chr4: 52,772,265-52,779,500 DCUN1D4
    nsv6725973copy number variation1nstd229human GRCh38 chr4: 51,908,327-51,908,514 , GRCh37.p13 chr4: 52,774,493-52,774,680 DCUN1D4
    nsv6720828copy number variation1nstd229human GRCh38 chr4: 51,905,385-52,362,727 , GRCh37.p13 chr4: 52,771,551-53,228,893 RPL37AP2, DCUN1D4, 5 more genes
    nsv6637063copy number variation1nstd102humanUncertain significance GRCh37 chr4: 52,685,980-59,272,025 , GRCh38.p12 chr4: 51,819,814-58,405,859 SPINK2, RN7SL492P, 100 more genes
    nsv6629495copy number variation1nstd224human GRCh37 chr4: 52,706,270-53,122,932 , GRCh38.p12 chr4: 51,840,104-52,256,766 SGCB, DCUN1D4, 5 more genes
    nsv6629446copy number variation15nstd224human GRCh37 chr4: 52,706,270-52,729,855 , GRCh38.p12 chr4: 51,840,104-51,863,689 DCUN1D4, DUTP7
    nsv6387232copy number variation1nstd223human GRCh38 chr4: 51,886,101-51,889,200 , GRCh37.p13 chr4: 52,752,267-52,755,366 DCUN1D4
    nsv6386411copy number variation1nstd223human GRCh38 chr4: 51,811,201-51,896,000 , GRCh37.p13 chr4: 52,677,367-52,762,166 DUTP7, DCUN1D4
    nsv6381611copy number variation1nstd223human GRCh38 chr4: 51,830,001-51,854,000 , GRCh37.p13 chr4: 52,696,167-52,720,166 DCUN1D4
    nsv6380554copy number variation1nstd223human GRCh38 chr4: 51,820,401-51,889,200 , GRCh37.p13 chr4: 52,686,567-52,755,366 DUTP7, DCUN1D4
    nsv6377101copy number variation1nstd223human GRCh38 chr4: 51,842,401-51,843,700 , GRCh37.p13 chr4: 52,708,567-52,709,866 DCUN1D4
    nsv6376081copy number variation1nstd223human GRCh38 chr4: 51,866,801-51,869,200 , GRCh37.p13 chr4: 52,732,967-52,735,366 DCUN1D4
    nsv6291206copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,685,685-58,104,722 , GRCh38.p12 chr4: 51,819,519-57,238,556 SRD5A3, DCUN1D4, 96 more genes
    nsv6244062mobile element insertion1nstd215human GRCh38 chr4: 51,897,588-51,897,588 , GRCh37.p13 chr4: 52,763,754-52,763,754 DCUN1D4
    nsv6158238copy number variation1nstd214human GRCh38 chr4: 51,894,216-51,894,273 , GRCh37.p13 chr4: 52,760,382-52,760,439 DCUN1D4
    nsv5839951copy number variation2nstd209human GRCh38 chr4: 51,912,108-51,913,544 , GRCh37.p13 chr4: 52,778,274-52,779,710 DCUN1D4
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