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Items: 1 to 20 of 105

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096524copy number variation1nstd102humanPathogenic GRCh37 chr2: 85,766,411-86,564,633 , GRCh38.p12 chr2: 85,539,288-86,337,510 GPR160P1, USP39, 27 more genes
    nsv7054602inversion1nstd229human GRCh38 chr2: 85,821,491-85,821,568 , GRCh37.p13 chr2: 86,048,614-86,048,691 LOC284950
    nsv6693992copy number variation1nstd229human GRCh38 chr2: 85,821,902-85,837,113 , GRCh37.p13 chr2: 86,049,025-86,064,236 ST3GAL5, LOC284950
    nsv6690517copy number variation1nstd229human GRCh38 chr2: 85,810,650-85,920,285 , GRCh37.p13 chr2: 86,037,773-86,147,408 ST3GAL5, LOC284950, 2 more genes
    nsv6688984copy number variation1nstd229human GRCh38 chr2: 85,788,849-86,014,059 , GRCh37.p13 chr2: 86,015,972-86,241,182 RN7SKP83, ST3GAL5-AS1, 4 more genes
    nsv6681244copy number variation1nstd229human GRCh38 chr2: 85,286,438-85,844,313 , GRCh37.p13 chr2: 85,513,561-86,071,436 RETSAT, SH2D6, 30 more genes
    nsv6679380copy number variation1nstd229human GRCh38 chr2: 85,824,442-85,828,204 , GRCh37.p13 chr2: 86,051,565-86,055,327 LOC284950
    nsv6636862copy number variation1nstd102humanUncertain significance GRCh37 chr2: 85,786,007-86,559,358 , GRCh38.p12 chr2: 85,558,884-86,332,235 MIR4779, RN7SKP83, 25 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6313890copy number variation1nstd102humanPathogenic GRCh37 chr2: 82,486,900-87,322,042 , GRCh38.p12 chr2: 82,259,776-87,094,919 LOC105374836, LOC105374833, 93 more genes
    nsv6112750copy number variation1nstd102humanPathogenic GRCh37 chr2: 81,209,244-86,688,030 , GRCh38.p12 chr2: 80,982,120-86,460,907 VAMP8, TMSB10, 86 more genes
    nsv5616926insertion1nstd207human GRCh38 chr2: 85,817,544-85,817,544 , GRCh37.p13 chr2: 86,044,667-86,044,667 LOC284950
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5436982copy number variation1nstd206human GRCh38 chr2: 85,539,948-89,142,574 , GRCh37.p13 chr2: 85,767,071-89,442,057 , IGKV2-18, 129 more genes
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4728539copy number variation1nstd102humanUncertain significance GRCh37 chr2: 85,786,006-86,559,358 , GRCh38.p12 chr2: 85,558,883-86,332,235 ST3GAL5-AS1, TMEM150A, 25 more genes
    nsv4519695copy number variation1nstd166human GRCh37.p13 chr2: 85,888,999-87,236,000 , GRCh38.p12 chr2: 85,661,876-87,008,877 , RNF103, 33 more genes
    nsv4453381copy number variation1nstd102humanUncertain significance GRCh37 chr2: 85,948,835-86,438,539 , GRCh38.p12 chr2: 85,721,712-86,211,416 MIR6071, MRPL35, 12 more genes
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