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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5194317mobile element insertion1nstd203human GRCh38 chr3: 185,495,612-185,495,612 , GRCh37.p13 chr3: 185,213,400-185,213,400 TMEM41A
    nsv4924956copy number variation1nstd200human GRCh38 chr3: 185,453,868-185,804,751 , GRCh37.p13 chr3: 185,171,656-185,522,539 , LIPH, 9 more genes
    nsv4728604copy number variation1nstd102humanPathogenic GRCh37 chr3: 182,877,291-186,830,759 , GRCh38.p12 chr3: 183,159,503-187,112,971 LOC105374253, GPS2P2, 111 more genes
    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
    nsv4674527copy number variation1nstd102humanUncertain significance GRCh37 chr3: 184,493,051-185,493,146 , GRCh38.p12 chr3: 184,775,263-185,775,358 LOC105374254, IGF2BP2-AS1, 16 more genes
    nsv4674171copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 183,789,584-186,034,649 , GRCh38.p12 chr3: 184,071,796-186,316,860 AP2M1, CLCN2, 54 more genes
    nsv4521752copy number variation1nstd166human GRCh37.p13 chr3: 185,112,998-185,749,000 , GRCh38.p12 chr3: 185,395,210-186,031,211 , TRA2B, 12 more genes
    nsv4367916copy number variation1nstd173human GRCh37 chr3: 184,400,855-185,981,810 , GRCh38.p12 chr3: 184,683,067-186,264,021 , RPL34P10, 25 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
    nsv4100329copy number variation1nstd166human GRCh37.p13 chr3: 185,216,760-185,216,972 , GRCh38.p12 chr3: 185,498,972-185,499,184 TMEM41A, LOC105374254
    nsv3968112insertion1nstd168human GRCh38 chr3: 185,475,199-185,494,297 , GRCh37.p13 chr3: 185,192,987-185,212,085 MAP3K13, TMEM41A, 1 more genes
    nsv3952425insertion1nstd167human GRCh37 chr3: 185,201,499-185,201,499 , GRCh38.p12 chr3: 185,483,711-185,483,711 MAP3K13, TMEM41A
    nsv3922577copy number variation1nstd102humanPathogenic GRCh37 chr3: 184,561,415-187,178,796 , GRCh38 chr3: 184,843,627-187,461,008 , NCBI36 chr3: 186,044,109-188,661,490 SNORA63, ADIPOQ-AS1, 59 more genes
    nsv3922385copy number variation1nstd102humanPathogenic NCBI36 chr3: 177,369,007-199,329,651 , GRCh37 chr3: 175,886,313-197,845,254 , GRCh38 chr3: 176,168,525-198,118,383 LINC02053, RTP4, 414 more genes
    nsv3920662copy number variation1nstd102humanPathogenic NCBI36 chr3: 178,729,187-199,321,446 , GRCh37.p13 chr3: 177,246,493-197,837,049 , GRCh38.p12 chr3: 177,528,705-198,110,178 RN7SKP265, RPL24P6, 401 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
    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
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