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Items: 1 to 20 of 160

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096446copy number variation1nstd102humanUncertain significance GRCh37 chr3: 155,570,992-155,571,786 , GRCh38.p12 chr3: 155,853,203-155,853,997 SLC33A1, LOC105374174
    nsv7047569inversion1nstd229human GRCh38 chr3: 152,490,812-161,531,961 , GRCh37.p13 chr3: 152,208,601-161,249,749 RPS2P19, LOC112268450, 128 more genes
    nsv6737959copy number variation1nstd229human GRCh38 chr3: 155,770,701-155,875,600 , GRCh37.p13 chr3: 155,488,490-155,593,389 GMPS, SLC33A1, 2 more genes
    nsv6734474copy number variation1nstd229human GRCh38 chr3: 155,748,615-155,963,900 , GRCh37.p13 chr3: 155,466,404-155,681,689 GMPS, SLC33A1, 3 more genes
    nsv6733722copy number variation1nstd229human GRCh38 chr3: 155,860,817-155,864,375 , GRCh37.p13 chr3: 155,578,606-155,582,164 LOC105374174
    nsv6724259copy number variation1nstd229human GRCh38 chr3: 155,780,401-155,875,500 , GRCh37.p13 chr3: 155,498,190-155,593,289 SLC33A1, C3orf33, 2 more genes
    nsv6724097copy number variation1nstd229human GRCh38 chr3: 155,859,341-156,259,331 , GRCh37.p13 chr3: 155,577,130-155,977,120 GMPS, SNRNP40P1, 7 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6628657copy number variation1nstd224human GRCh37 chr3: 155,412,668-155,571,275 , GRCh38.p12 chr3: 155,694,879-155,853,486 SLC33A1, PLCH1, 3 more genes
    nsv6563804inversion1nstd223human GRCh38 chr3: 155,855,485-155,855,830 , GRCh37.p13 chr3: 155,573,274-155,573,619 LOC105374174, SLC33A1
    nsv6366376copy number variation1nstd223human GRCh38 chr3: 155,746,388-156,594,198 , GRCh37.p13 chr3: 155,464,177-156,311,987 SNRNP40P1, MRE11P1, 12 more genes
    nsv6313678copy number variation1nstd102humanPathogenic GRCh37 chr3: 145,486,960-160,504,834 , GRCh38.p12 chr3: 145,769,173-160,787,046 RNU6-901P, RPL32P8, 229 more genes
    nsv6313655copy number variation1nstd102humanUncertain significance GRCh37 chr3: 155,464,751-155,599,910 , GRCh38.p12 chr3: 155,746,962-155,882,121 RPL7AP24, GMPS, 3 more genes
    nsv6290273copy number variation1nstd102humanPathogenic GRCh37 chr3: 142,729,607-157,921,084 , GRCh38.p12 chr3: 143,010,765-158,203,295 LINC02066, TM4SF1-AS1, 206 more genes
    nsv6290244copy number variation1nstd102humanPathogenic GRCh37 chr3: 143,439,359-165,252,122 , GRCh38.p12 chr3: 143,720,517-165,534,334 LOC102724145, C3orf80, 273 more genes
    nsv6134788copy number variation1nstd213human GRCh37 chr3: 155,010,000-169,630,001 , GRCh38.p12 chr3: 155,292,211-169,912,213 , BCHE, 171 more genes
    nsv5991691copy number variation1nstd212human GRCh38 chr3: 155,862,970-155,863,073 , GRCh37.p13 chr3: 155,580,759-155,580,862 LOC105374174
    nsv5681756mobile element insertion2nstd211human GRCh38 chr3: 155,856,924-155,856,924 , GRCh37.p13 chr3: 155,574,713-155,574,713 LOC105374174
    nsv5445714copy number variation1nstd206human GRCh38 chr3: 154,528,533-156,057,304 , GRCh37.p13 chr3: 154,246,322-155,775,093 LINC01487, MME, 21 more genes
    nsv5408116mobile element insertion1nstd206human GRCh38 chr3: 155,856,924-155,856,975 , GRCh37.p13 chr3: 155,574,713-155,574,764 LOC105374174
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