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Items: 1 to 20 of 117

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112673copy number variation1nstd102humanPathogenic GRCh37 chr2: 88,007,281-90,260,248 , GRCh38.p12 chr2: 87,707,762-90,221,382 IGKV3-20, IGKV3-7, 122 more genes
    nsv5882908copy number variation1nstd209human GRCh38 chr2: 88,315,331-88,598,001 , GRCh37.p13 chr2: 88,614,850-88,897,519 EIF2AK3, SPMIP9, 6 more genes
    nsv5834084copy number variation1nstd209human GRCh38 chr2: 88,361,292-88,377,018 , GRCh37.p13 chr2: 88,660,811-88,676,537 MRPL45P1
    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
    nsv4902438copy number variation1nstd200human GRCh38 chr2: 88,358,017-88,364,398 , GRCh37.p13 chr2: 88,657,536-88,663,917 MRPL45P1
    nsv4894688copy number variation1nstd200human GRCh38 chr2: 88,363,469-88,368,265 , GRCh37.p13 chr2: 88,662,988-88,667,784 MRPL45P1
    nsv4776942copy number variation1nstd200human GRCh37 chr2: 88,657,536-88,663,917 , GRCh38.p12 chr2: 88,358,017-88,364,398 MRPL45P1
    nsv4766632inversion1nstd199human GRCh37 chr2: 87,997,505-112,010,501 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,697,986-111,252,924 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 706 more genes
    nsv4752571inversion1nstd199human GRCh37 chr2: 87,550,795-112,295,517 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,323,672-111,537,940 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 723 more genes
    nsv4743379copy number variation1nstd199human GRCh37 chr2: 88,481,090-124,440,189 , GRCh38.p12 chr9: 40,649,751-63,450,622 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 88,181,571-123,682,613 , EIF2AK3, 861 more genes
    nsv4674077copy number variation1nstd102humanUncertain significance GRCh37 chr2: 88,403,403-89,129,064 , GRCh38.p12 chr2: 88,103,884-88,829,551 EIF2AK3, LOC101928347, 19 more genes
    nsv4595834copy number variation1nstd183human GRCh37 chr2: 87,737,295-89,320,921 , GRCh38.p12 chr2: 87,441,084-89,021,424 , FABP1, 61 more genes
    nsv4519925copy number variation1nstd166human GRCh37.p13 chr2: 88,557,999-89,254,000 , GRCh38.p12 chr2: 88,258,480-88,954,481 , MALLP2, 29 more genes
    nsv4068874copy number variation1nstd166human GRCh37.p13 chr2: 88,658,107-88,662,806 , GRCh38.p12 chr2: 88,358,588-88,363,287 MRPL45P1
    nsv4059277copy number variation1nstd166human GRCh37.p13 chr2: 88,658,000-88,663,000 , GRCh38.p12 chr2: 88,358,481-88,363,481 MRPL45P1
    nsv3918504copy number variation1nstd102humanUncertain significance NCBI36 chr2: 88,421,181-88,553,792 , GRCh37.p13 chr2: 88,640,066-88,772,677 , GRCh38.p12 chr2: 88,340,547-88,473,159 MRPL45P1, RNU6-1168P, 3 more genes
    nsv3910630copy number variation1nstd102humanPathogenic NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331 DAZAP2P1, RPL36AP16, 2991 more genes
    nsv3909593copy number variation1nstd102humanUncertain significance GRCh37 chr2: 87,602,598-91,619,262 , NCBI36 chr2: 87,456,109-90,982,989 , GRCh38 chr2: 87,375,475-90,282,666 LOC101928371, IGKV1-32, 130 more genes
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