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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    nsv5436299copy number variation1nstd206human GRCh38 chr2: 86,055,590-86,283,810 , GRCh37.p13 chr2: 86,282,713-86,510,933 IMMT, POLR1A, 5 more genes
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4908905copy number variation1nstd200human GRCh38 chr2: 86,055,590-86,283,810 , GRCh37.p13 chr2: 86,282,713-86,510,933 IMMT, PTCD3, 5 more genes
    nsv4781632copy number variation1nstd200human GRCh37 chr2: 86,282,713-86,510,933 , GRCh38.p12 chr2: 86,055,590-86,283,810 SNORD94, PTCD3, 5 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
    nsv4674016copy number variation1nstd102humanUncertain significance GRCh37 chr2: 86,286,478-86,516,984 , GRCh38.p12 chr2: 86,059,355-86,289,861 SNORD94, IMMT, 5 more genes
    nsv4586731copy number variation1nstd183human GRCh37 chr2: 86,282,734-86,517,030 , GRCh38.p12 chr2: 86,055,611-86,289,907 IMMT, POLR1A, 5 more genes
    nsv4584245copy number variation1nstd183human GRCh37 chr2: 86,403,814-86,506,144 , GRCh38.p12 chr2: 86,176,691-86,279,021 REEP1, IMMT, 2 more genes
    nsv4584244copy number variation1nstd183human GRCh37 chr2: 86,285,812-86,509,326 , GRCh38.p12 chr2: 86,058,689-86,282,203 IMMT, POLR1A, 5 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
    nsv4451607copy number variation1nstd102humanPathogenic GRCh37 chr2: 77,907,114-87,330,965 , GRCh38.p12 chr2: 77,679,988-87,103,842 REEP1, RBX1P1, 134 more genes
    nsv4405121copy number variation1nstd174human GRCh37 chr2: 86,281,967-86,510,932 , GRCh38.p12 chr2: 86,054,844-86,283,809 IMMT, POLR1A, 5 more genes
    nsv4369330copy number variation1nstd173human GRCh37 chr2: 86,282,906-86,516,984 , GRCh38.p12 chr2: 86,055,783-86,289,861 POLR1A, PTCD3, 5 more genes
    nsv4071536copy number variation1nstd166human GRCh37.p13 chr2: 86,282,713-86,510,933 , GRCh38.p12 chr2: 86,055,590-86,283,810 IMMT, POLR1A, 5 more genes
    nsv3967089copy number variation1nstd168human GRCh38 chr2: 86,139,513-86,225,580 , GRCh37.p13 chr2: 86,366,636-86,452,703 PTCD3, REEP1, 3 more genes
    nsv3919539copy number variation1nstd102humanUncertain significance NCBI36 chr2: 86,114,440-86,387,285 , GRCh37.p13 chr2: 86,260,929-86,533,774 , GRCh38.p12 chr2: 86,033,806-86,306,651 SNORD94, PTCD3, 5 more genes
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