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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5891126copy number variation1nstd209human GRCh38 chr5: 111,081,251-111,111,530 , GRCh37.p13 chr5: 110,416,949-110,447,229 WDR36
    nsv5840351copy number variation1nstd209human GRCh38 chr5: 111,081,858-111,103,585 , GRCh37.p13 chr5: 110,417,556-110,439,284 WDR36
    nsv5562865sequence alteration1nstd206human GRCh38 chr5: 111,127,776-111,128,715 , GRCh37.p13 chr5: 110,463,474-110,464,413 WDR36
    nsv5547934insertion1nstd206human GRCh38 chr5: 111,127,919-111,127,919 , GRCh37.p13 chr5: 110,463,617-110,463,617 WDR36
    nsv5472444copy number variation1nstd206human GRCh38 chr5: 111,081,251-111,111,534 , GRCh37.p13 chr5: 110,416,949-110,447,233 WDR36
    nsv5464023copy number variation1nstd206human GRCh38 chr5: 110,989,807-111,303,807 , GRCh37.p13 chr5: 110,325,506-110,639,505 CAMK4, TSLP, 4 more genes
    nsv5463199copy number variation1nstd206human GRCh38 chr5: 111,123,177-111,123,307 , GRCh37.p13 chr5: 110,458,875-110,459,005 WDR36
    nsv5316118copy number variation1nstd204human GRCh38.p13 chr5: 111,081,245-111,111,543 , GRCh37.p13 chr5: 110,416,943-110,447,242 WDR36
    nsv5234697copy number variation1nstd204human GRCh38.p13 chr5: 111,086,428-111,090,867 , GRCh37.p13 chr5: 110,422,126-110,426,565 WDR36
    nsv5224138copy number variation1nstd204human GRCh38.p13 chr5: 111,081,058-111,100,985 , GRCh37.p13 chr5: 110,416,756-110,436,684 WDR36
    nsv5222714copy number variation1nstd204human GRCh38.p13 chr5: 111,081,358-111,112,355 , GRCh37.p13 chr5: 110,417,056-110,448,054 WDR36
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5034346inversion1nstd200human GRCh38 chr5: 99,223,339-135,778,784 , GRCh37.p13 chr5: 98,559,043-135,114,473 , NUDT12, 438 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4944924copy number variation1nstd200human GRCh38 chr5: 111,081,251-111,111,534 , GRCh37.p13 chr5: 110,416,949-110,447,233 WDR36
    nsv4932219copy number variation1nstd200human GRCh38 chr5: 111,117,016-111,117,325 , GRCh37.p13 chr5: 110,452,714-110,453,023 WDR36
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4872282inversion1nstd200human GRCh37 chr5: 98,106,197-132,803,784 , GRCh38.p12 chr5: 98,770,493-133,468,092 , LEAP2, 395 more genes
    nsv4805740copy number variation1nstd200human GRCh37 chr5: 110,416,949-110,447,233 , GRCh38.p12 chr5: 111,081,251-111,111,534 WDR36
    nsv4729561copy number variation1nstd102humanUncertain significance GRCh37 chr5: 110,338,499-110,668,272 , GRCh38.p12 chr5: 111,002,800-111,332,574 LOC100129099, WDR36, 4 more genes
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