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Items: 1 to 20 of 159

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054051inversion1nstd229human GRCh38 chr3: 151,747,093-152,168,059 , GRCh37.p13 chr3: 151,464,881-151,885,848 LOC107986047, AADAC, 6 more genes
    nsv6737482copy number variation1nstd229human GRCh38 chr3: 151,870,472-151,874,204 , GRCh37.p13 chr3: 151,588,260-151,591,992 AADACL2-AS1, SUCNR1
    nsv6732714copy number variation1nstd229human GRCh38 chr3: 151,883,465-151,894,229 , GRCh37.p13 chr3: 151,601,253-151,612,017 SUCNR1, LOC105374159, 1 more genes
    nsv6727932copy number variation1nstd229human GRCh38 chr3: 151,827,801-151,875,000 , GRCh37.p13 chr3: 151,545,589-151,592,788 AADACL2-AS1, AADAC, 1 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
    nsv6628462copy number variation1nstd224human GRCh37 chr3: 151,597,310-151,708,414 , GRCh38.p12 chr3: 151,879,522-151,990,625 LOC105374159, LOC107986047, 2 more genes
    nsv6374967copy number variation1nstd223human GRCh38 chr3: 151,874,701-151,875,800 , GRCh37.p13 chr3: 151,592,489-151,593,588 SUCNR1, AADACL2-AS1
    nsv6374217copy number variation1nstd223human GRCh38 chr3: 151,883,470-151,894,224 , GRCh37.p13 chr3: 151,601,258-151,612,012 LOC105374159, AADACL2-AS1, 1 more genes
    nsv6372024copy number variation1nstd223human GRCh38 chr3: 151,876,388-151,876,923 , GRCh37.p13 chr3: 151,594,176-151,594,711 AADACL2-AS1, SUCNR1
    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
    nsv6313632copy number variation1nstd102humanUncertain significance GRCh37 chr3: 151,147,204-154,845,718 , GRCh38.p12 chr3: 151,429,416-155,127,929 LOC105374171, ARHGEF26-AS1, 42 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
    nsv6151203copy number variation1nstd214human GRCh38 chr3: 151,884,835-151,885,001 , GRCh37.p13 chr3: 151,602,623-151,602,789 SUCNR1, AADACL2-AS1
    nsv6134674copy number variation1nstd213human GRCh37 chr3: 150,600,000-153,170,001 , GRCh38.p12 chr3: 150,882,213-153,452,212 CLRN1-AS1, MBNL1-AS1, 37 more genes
    nsv5991614copy number variation1nstd212human GRCh38 chr3: 151,884,743-151,884,902 , GRCh37.p13 chr3: 151,602,531-151,602,690 AADACL2-AS1, SUCNR1
    nsv5674442mobile element insertion2nstd211human GRCh38 chr3: 151,878,035-151,878,035 , GRCh37.p13 chr3: 151,595,823-151,595,823 AADACL2-AS1, SUCNR1
    nsv5413469mobile element insertion1nstd206human GRCh38 chr3: 151,878,035-151,878,086 , GRCh37.p13 chr3: 151,595,823-151,595,874 AADACL2-AS1, SUCNR1
    nsv5381765copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911 MBNL1-AS1, LOC107986138, 339 more genes
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
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