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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
    nsv4769329copy number variation1nstd102humanPathogenic GRCh37 chr3: 180,102,701-181,991,155 , GRCh38.p12 chr3: 180,384,913-182,273,367 TTC14, RPL32P10, 24 more genes
    nsv4769323copy number variation1nstd102humanPathogenic GRCh37 chr3: 180,913,778-181,432,287 , GRCh38.p12 chr3: 181,195,990-181,714,499 SOX2, SOX2-OT, 4 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
    nsv4728751copy number variation1nstd102humanPathogenic GRCh37 chr3: 179,016,729-181,527,320 , GRCh38.p12 chr3: 179,298,941-181,809,532 PEX5L, NDUFB5, 33 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
    nsv4674507copy number variation1nstd102humanPathogenic GRCh37 chr3: 180,510,432-181,562,798 , GRCh38.p12 chr3: 180,792,644-181,845,010 DNAJC19, FXR1, 13 more genes
    nsv4674364copy number variation1nstd102humanPathogenic GRCh37 chr3: 181,386,449-181,504,204 , GRCh38.p12 chr3: 181,668,661-181,786,416 SOX2-OT, SOX2
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 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
    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
    nsv3917522copy number variation1nstd102humanBenign NCBI36 chr3: 182,912,642-182,913,647 , GRCh37 chr3: 181,429,948-181,430,953 , GRCh38 chr3: 181,712,160-181,713,165 SOX2, SOX2-OT
    nsv3917117copy number variation1nstd102humanPathogenic NCBI36 chr3: 182,889,729-182,994,598 , GRCh38 chr3: 181,689,247-181,794,116 , GRCh37 chr3: 181,407,035-181,511,904 SOX2, SOX2-OT
    nsv3915871copy number variation1nstd102humanBenign NCBI36 chr3: 182,845,473-182,952,205 , GRCh37 chr3: 181,362,779-181,469,511 , GRCh38 chr3: 181,644,991-181,751,723 SOX2, SOX2-OT
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