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Items: 1 to 20 of 144

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144159copy number variation1nstd232human GRCh37.p13 chr3: 156,867,766-156,867,852 , GRCh38.p12 chr3: 157,149,977-157,150,063 CCNL1
    nsv7047569inversion1nstd229human GRCh38 chr3: 152,490,812-161,531,961 , GRCh37.p13 chr3: 152,208,601-161,249,749 RPS2P19, LOC112268450, 128 more genes
    nsv6734371copy number variation1nstd229human GRCh38 chr3: 156,578,264-157,290,961 , GRCh37.p13 chr3: 156,296,053-157,008,750 PA2G4P4, METTL15P1, 17 more genes
    nsv6732334copy number variation1nstd229human GRCh38 chr3: 157,137,401-157,145,200 , GRCh37.p13 chr3: 156,855,190-156,862,989 CCNL1
    nsv6730096copy number variation1nstd229human GRCh38 chr3: 157,143,580-157,146,356 , GRCh37.p13 chr3: 156,861,369-156,864,145 CCNL1
    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
    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
    nsv6313664copy number variation1nstd102humanUncertain significance GRCh37 chr3: 156,768,935-160,158,553 , GRCh38.p12 chr3: 157,051,146-160,440,765 LOC105374179, RPL15P6, 49 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
    nsv6072672insertion1nstd212human GRCh38 chr3: 157,156,607-157,156,607 , GRCh37.p13 chr3: 156,874,396-156,874,396 CCNL1
    nsv5441859copy number variation1nstd206human GRCh38 chr3: 157,156,692-157,175,504 , GRCh37.p13 chr3: 156,874,481-156,893,293 CCNL1, KRT18P34, 2 more genes
    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
    nsv5081300mobile element insertion1nstd203human GRCh38 chr3: 157,145,437-157,145,464 , GRCh37.p13 chr3: 156,863,226-156,863,253 CCNL1
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4912582copy number variation1nstd200human GRCh38 chr3: 157,143,580-157,146,352 , GRCh37.p13 chr3: 156,861,369-156,864,141 CCNL1
    nsv4684209copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,145,289-162,275,610 , GRCh38.p12 chr3: 138,426,447-162,557,822 MTAPP1, PLS1, 339 more genes
    nsv4684148copy number variation1nstd102humanUncertain significance GRCh37 chr3: 156,812,581-160,154,747 , GRCh38.p12 chr3: 157,094,792-160,436,959 RSRC1, SMC4, 48 more genes
    nsv4587640copy number variation1nstd183human GRCh37 chr3: 156,874,767-156,882,274 , GRCh38.p12 chr3: 157,156,978-157,164,485 KRT18P34, CCNL1
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