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Items: 1 to 20 of 156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5896500copy number variation1nstd209human GRCh38 chr3: 171,525,972-180,293,041 , GRCh37.p13 chr3: 171,243,761-180,010,829 , RNU6-1120P, 95 more genes
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4920726copy number variation1nstd200human GRCh38 chr3: 172,523,670-172,531,730 , GRCh37.p13 chr3: 172,241,460-172,249,520 TNFSF10
    nsv4920725copy number variation1nstd200human GRCh38 chr3: 172,523,357-172,527,662 , GRCh37.p13 chr3: 172,241,147-172,245,452 TNFSF10, TBPL1P1
    nsv4798577copy number variation1nstd200human GRCh37 chr3: 172,241,459-172,249,520 , GRCh38.p12 chr3: 172,523,669-172,531,730 TNFSF10
    nsv4674680copy number variation1nstd102humanPathogenic GRCh37 chr3: 169,617,690-190,593,854 , GRCh38.p12 chr3: 169,899,902-190,876,065 RNU6-1120P, LOC105374262, 323 more genes
    nsv4558201mobile element insertion1nstd166human GRCh37.p13 chr3: 172,222,049-172,222,049 , GRCh38.p12 chr3: 172,504,259-172,504,259 TNFSF10
    nsv4451456copy number variation1nstd102humanUncertain significance GRCh37 chr3: 172,095,903-173,254,604 , GRCh38.p12 chr3: 172,378,113-173,536,814 TBPL1P1, RNU6-547P, 17 more genes
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4106944copy number variation1nstd166human GRCh37.p13 chr3: 172,232,892-172,243,200 , GRCh38.p12 chr3: 172,515,102-172,525,410 TBPL1P1, TNFSF10
    nsv3970177insertion1nstd168human GRCh38 chr3: 172,509,380-172,516,921 , GRCh37.p13 chr3: 172,227,170-172,234,711 TNFSF10
    nsv3965560copy number variation1nstd168human GRCh38 chr3: 172,516,921-172,560,227 , GRCh37.p13 chr3: 172,234,711-172,278,017 TBPL1P1, TNFSF10, 1 more genes
    nsv3919833copy number variation1nstd102humanPathogenic GRCh38 chr3: 158,141,556-172,788,324 , NCBI36 chr3: 159,342,039-173,988,808 , GRCh37 chr3: 157,859,345-172,506,114 NMD3, TRV-AAC1-1, 173 more genes
    nsv3918982copy number variation1nstd102humanPathogenic GRCh37 chr3: 167,885,356-197,837,049 , NCBI36 chr3: 169,368,050-199,321,446 , GRCh38 chr3: 168,167,568-198,110,178 EIF4G1, LOC105374248, 515 more genes
    nsv3918981copy number variation1nstd102humanPathogenic GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446 LINC02614, LINC02054, 1469 more genes
    nsv3918784copy number variation1nstd102humanPathogenic GRCh37 chr3: 147,160,353-178,240,319 , GRCh38 chr3: 147,442,566-178,522,531 , NCBI36 chr3: 148,643,043-179,723,013 LOC105374167, LOC105374187, 394 more genes
    nsv3918692copy number variation1nstd102humanPathogenic GRCh38 chr3: 147,521,892-198,096,565 , GRCh37 chr3: 147,239,679-197,823,436 , NCBI36 chr3: 148,722,369-199,307,833 LOC105374179, LINC02038, 785 more genes
    nsv3918149copy number variation1nstd102humanPathogenic GRCh37 chr3: 155,836,230-197,851,986 , GRCh38 chr3: 156,118,441-198,125,115 , NCBI36 chr3: 157,318,924-199,336,383 LINC02031, PCBP2P4, 647 more genes
    nsv3918066copy number variation1nstd102humanPathogenic GRCh38 chr3: 152,100,512-198,118,383 , NCBI36 chr3: 153,300,991-199,329,651 , GRCh37 chr3: 151,818,301-197,845,254 LOC105374260, LOC105374174, 696 more genes
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