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Items: 1 to 20 of 143

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6732771copy number variation1nstd229human GRCh38 chr3: 151,043,625-151,381,082 , GRCh37.p13 chr3: 150,761,412-151,098,870 CLRN1-AS1, P2RY12, 7 more genes
    nsv6723612copy number variation1nstd229human GRCh38 chr3: 151,171,594-151,371,171 , GRCh37.p13 chr3: 150,889,381-151,088,959 GPR87, P2RY12, 6 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
    nsv6368434copy number variation1nstd223human GRCh38 chr3: 151,199,974-151,200,593 , GRCh37.p13 chr3: 150,917,761-150,918,380 GPR171, MED12L
    nsv6356250copy number variation1nstd223human GRCh38 chr3: 151,178,849-151,449,476 , GRCh37.p13 chr3: 150,896,636-151,167,264 GPR171, RNA5SP145, 7 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
    nsv6311444copy number variation1nstd102humanPathogenic GRCh37 chr3: 148,447,967-151,176,497 , GRCh38.p12 chr3: 148,730,180-151,458,709 TM4SF1, FKBP1AP4, 68 more genes
    nsv6291181copy number variation1nstd102humanUncertain significance GRCh37 chr3: 150,889,080-151,090,963 , GRCh38.p12 chr3: 151,171,293-151,373,175 P2RY14, GPR87, 6 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
    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
    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
    nsv4797992copy number variation1nstd200human GRCh37 chr3: 150,889,381-151,088,954 , GRCh38.p12 chr3: 151,171,594-151,371,166 P2RY14, GPR171, 6 more genes
    nsv4728674copy number variation1nstd102humanUncertain significance GRCh37 chr3: 150,898,920-151,165,339 , GRCh38.p12 chr3: 151,181,133-151,447,551 P2RY14, RNA5SP145, 7 more genes
    nsv4728613copy number variation1nstd102humanLikely benign GRCh37 chr3: 150,898,716-151,133,816 , GRCh38.p12 chr3: 151,180,929-151,416,028 GPR87, P2RY12, 6 more genes
    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
    nsv4674301copy number variation1nstd102humanPathogenic GRCh37 chr3: 149,404,255-152,786,331 , GRCh38.p12 chr3: 149,686,468-153,068,542 EIF3JP2, IGSF10, 63 more genes
    nsv4673991copy number variation1nstd102humanUncertain significance GRCh37 chr3: 150,534,295-151,213,925 , GRCh38.p12 chr3: 150,816,508-151,496,137 P2RY14, RNA5SP145, 11 more genes
    nsv4469442mobile element insertion1nstd166human GRCh37.p13 chr3: 150,913,733-150,913,733 , GRCh38.p12 chr3: 151,195,946-151,195,946 GPR171, MED12L
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