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Items: 1 to 20 of 186

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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
    nsv5870963copy number variation1nstd209human GRCh38 chr2: 88,522,439-88,522,963 , GRCh37.p13 chr2: 88,821,957-88,822,481 SPMIP9
    nsv5868418copy number variation1nstd209human GRCh38 chr2: 88,528,294-88,531,931 , GRCh37.p13 chr2: 88,827,812-88,831,449 SPMIP9
    nsv5834101copy number variation2nstd209human GRCh38 chr2: 88,526,810-88,531,634 , GRCh37.p13 chr2: 88,826,328-88,831,152 SPMIP9
    nsv5834100copy number variation2nstd209human GRCh38 chr2: 88,525,334-88,542,565 , GRCh37.p13 chr2: 88,824,852-88,842,083 SPMIP9, LOC101928371
    nsv5834099copy number variation1nstd209human GRCh38 chr2: 88,523,280-88,525,583 , GRCh37.p13 chr2: 88,822,798-88,825,101 SPMIP9
    nsv5576138copy number variation1nstd207human GRCh38 chr2: 88,522,448-88,522,970 , GRCh37.p13 chr2: 88,821,966-88,822,488 SPMIP9
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5450089copy number variation1nstd206human GRCh38 chr2: 88,528,152-88,532,190 , GRCh37.p13 chr2: 88,827,670-88,831,708 SPMIP9
    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
    nsv5435999copy number variation1nstd206human GRCh38 chr2: 88,522,439-88,522,971 , GRCh37.p13 chr2: 88,821,957-88,822,489 SPMIP9
    nsv5384741copy number variation2nstd186human GRCh37 chr2: 88,821,957-88,822,489 , GRCh38.p12 chr2: 88,522,439-88,522,971 SPMIP9
    nsv5384463copy number variation1nstd186human GRCh37 chr2: 88,827,758-88,831,511 , GRCh38.p12 chr2: 88,528,240-88,531,993 SPMIP9
    nsv5382243copy number variation1nstd186human GRCh37 chr2: 88,827,757-88,831,503 , GRCh38.p12 chr2: 88,528,239-88,531,985 SPMIP9
    nsv5284942copy number variation1nstd204human GRCh38.p13 chr2: 88,522,439-88,522,971 , GRCh37.p13 chr2: 88,821,957-88,822,489 SPMIP9
    nsv5206023copy number variation1nstd204human GRCh38.p13 chr2: 88,522,401-88,523,000 , GRCh37.p13 chr2: 88,821,919-88,822,518 SPMIP9
    nsv5202873copy number variation1nstd204human GRCh38.p13 chr2: 88,528,210-88,531,834 , GRCh37.p13 chr2: 88,827,728-88,831,352 SPMIP9
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4902452copy number variation1nstd200human GRCh38 chr2: 88,529,887-88,535,511 , GRCh37.p13 chr2: 88,829,405-88,835,029 SPMIP9
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