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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148131copy number variation1nstd102humanPathogenic GRCh37 chr8: 10,501-11,142,629 , GRCh38.p12 chr8: 60,501-11,285,120 XKR6, FAM90A11, 224 more genes
    nsv7148128copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 10,501-6,614,959 , GRCh38.p12 chr8: 60,501-6,757,438 ANGPT2, CLN8, 67 more genes
    nsv6290263copy number variation1nstd102humanPathogenic GRCh37 chr8: 10,501-7,214,947 , GRCh38.p12 chr8: 60,501-7,357,425 LOC105379585, VPS51P8, 108 more genes
    nsv6142865copy number variation1nstd206human GRCh38 chr8: 148,000-734,000 , GRCh37.p13 chr8: 98,000-684,000 ZNF596, RPL23AP53, 9 more genes
    nsv6137304copy number variation1nstd213human GRCh37 chr8: 80,000-2,190,001 , GRCh38.p12 chr8: 130,000-2,017,223 KBTBD11, LOC286083, 29 more genes
    nsv6136656copy number variation1nstd213human GRCh37 chr8: 1-7,470,001 , GRCh38.p12 chr8: 60,001-7,612,479 ANGPT2, DEFA1, 128 more genes
    nsv6136027copy number variation2nstd213human GRCh37 chr8: 1-2,200,001 , GRCh38.p12 chr8: 60,001-2,017,223 CLN8, DLGAP2, 30 more genes
    nsv5485583copy number variation1nstd206human GRCh38 chr8: 146,000-462,000 , GRCh37.p13 chr8: 96,000-412,000 FBXO25, FAM87A, 7 more genes
    nsv5258960copy number variation1nstd204human GRCh38.p13 chr8: 165,101-168,300 , GRCh37.p13 chr8: 115,101-118,300 OR4F21
    nsv5258697copy number variation1nstd204human GRCh38.p13 chr8: 166,801-168,400 , GRCh37.p13 chr8: 116,801-118,400 OR4F21
    nsv5257001copy number variation1nstd204human GRCh38.p13 chr8: 159,701-196,200 , GRCh37.p13 chr8: 109,701-146,200 OR4F21
    nsv5255954copy number variation1nstd204human GRCh38.p13 chr8: 165,101-174,600 , GRCh37.p13 chr8: 115,101-124,600 OR4F21
    nsv5251149copy number variation1nstd204human GRCh38.p13 chr8: 166,801-205,300 , GRCh37.p13 chr8: 116,801-155,300 SEPTIN14P8, OR4F21
    nsv5249800copy number variation1nstd204human GRCh38.p13 chr8: 94,801-205,300 , GRCh37.p13 chr8: 44,801-155,300 OR4F21, SEPTIN14P8, 2 more genes
    nsv5247469copy number variation1nstd204human GRCh38.p13 chr8: 166,801-174,600 , GRCh37.p13 chr8: 116,801-124,600 OR4F21
    nsv5245436copy number variation1nstd204human GRCh38.p13 chr8: 163,701-176,900 , GRCh37.p13 chr8: 113,701-126,900 OR4F21
    nsv4708622copy number variation1nstd195human GRCh37 chr8: 114,551-115,151 , GRCh38.p12 chr8: 164,551-165,151 OR4F21
    nsv4679895copy number variation1nstd189human GRCh37.p13 chr8: 1-440,940 , GRCh38.p12 chr8: 60,001-490,940 FBXO25, FAM87A, 9 more genes
    nsv4652103copy number variation1nstd186human GRCh37 chr8: 101,000-115,650 , GRCh38.p12 chr8: 151,000-165,650 OR4F21, WBP1LP3
    nsv4636003copy number variation1nstd186human GRCh37 chr8: 116,100-129,200 , GRCh38.p12 chr8: 166,100-179,200 OR4F21
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