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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
    nsv5948512insertion1nstd209human GRCh38 chr3: 183,149,575-183,149,575 , GRCh37.p13 chr3: 182,867,363-182,867,363 LAMP3
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5451852copy number variation1nstd206human GRCh38 chr3: 183,134,673-183,205,635 , GRCh37.p13 chr3: 182,852,461-182,923,423 SNORD3P4, LAMP3, 1 more genes
    nsv4805048copy number variation1nstd200human GRCh37 chr3: 182,880,789-182,885,188 , GRCh38.p12 chr3: 183,163,001-183,167,400 LAMP3
    nsv4805047copy number variation1nstd200human GRCh37 chr3: 182,863,442-182,864,991 , GRCh38.p12 chr3: 183,145,654-183,147,203 LAMP3
    nsv4798864copy number variation1nstd200human GRCh37 chr3: 182,854,773-182,855,068 , GRCh38.p12 chr3: 183,136,985-183,137,280 LAMP3
    nsv4777940mobile element deletion1nstd200human GRCh37 chr3: 182,869,215-182,869,514 , GRCh38.p12 chr3: 183,151,427-183,151,726 LAMP3
    nsv4769326copy number variation1nstd102humanPathogenic GRCh37 chr3: 182,871,341-182,987,855 , GRCh38.p12 chr3: 183,153,553-183,270,067 LAMP3, RNA5SP151, 3 more genes
    nsv4769308copy number variation1nstd102humanPathogenic GRCh37 chr3: 180,834,336-183,551,661 , GRCh38.p12 chr3: 181,116,548-183,833,873 SNORD3P4, B3GNT5, 43 more genes
    nsv4769252copy number variation1nstd102humanPathogenic GRCh37 chr3: 181,171,210-184,706,091 , GRCh38.p12 chr3: 181,453,422-184,988,303 LOC107986054, LOC107986160, 83 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
    nsv4570350mobile element insertion1nstd166human GRCh37.p13 chr3: 182,863,126-182,863,126 , GRCh38.p12 chr3: 183,145,338-183,145,338 LAMP3
    nsv4452071copy number variation1nstd102humanUncertain significance GRCh37 chr3: 182,787,792-182,922,112 , GRCh38.p12 chr3: 183,070,004-183,204,324 MCF2L2, LAMP3, 3 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
    nsv4298779insertion1nstd166human GRCh37.p13 chr3: 182,846,858-182,846,858 , GRCh38.p12 chr3: 183,129,070-183,129,070 LAMP3
    nsv4108652copy number variation1nstd166human GRCh37.p13 chr3: 182,864,000-182,874,000 , GRCh38.p12 chr3: 183,146,212-183,156,212 LAMP3
    nsv4102016copy number variation1nstd166human GRCh37.p13 chr3: 182,852,461-182,923,423 , GRCh38.p12 chr3: 183,134,673-183,205,635 LAMP3, MCF2L2, 1 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
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