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Items: 1 to 20 of 81

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6634512copy number variation1nstd102humanPathogenic GRCh38 chr3: 179,547,548-182,152,788 , GRCh37.p13 chr3: 179,265,336-181,870,576 LOC105374243, RNF13P1, 34 more genes
    nsv6634384copy number variation1nstd102humanPathogenic GRCh37 chr3: 181,062,175-185,474,509 , GRCh38.p12 chr3: 181,344,387-185,756,721 PRICKLE1P1, KLHL24, 99 more genes
    nsv6634371copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 171,549,421-198,022,430 , GRCh38.p12 chr3: 171,831,631-198,235,559 ACTL6A, AHSG, 466 more genes
    nsv6369980copy number variation1nstd223human GRCh38 chr3: 181,711,501-181,713,100 , GRCh37.p13 chr3: 181,429,289-181,430,888 SOX2, SOX2-OT
    nsv6363905copy number variation1nstd223human GRCh38 chr3: 181,692,501-181,733,000 , GRCh37.p13 chr3: 181,410,289-181,450,788 SOX2-OT, SOX2
    nsv6290246copy number variation1nstd102humanPathogenic GRCh37 chr3: 175,119,199-187,592,480 , GRCh38.p12 chr3: 175,401,410-187,874,692 RPL39L, MCF2L2, 220 more genes
    nsv6135004copy number variation1nstd213human GRCh37 chr3: 180,650,000-182,180,001 , GRCh38.p12 chr3: 180,932,212-182,462,213 , SOX2, 15 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
    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
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