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Items: 1 to 20 of 130

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv6896035copy number variation1nstd229human GRCh38 chr10: 118,232,592-118,246,871 , GRCh37.p13 chr10: 119,992,104-120,006,383 LINC02944
    nsv6892830copy number variation1nstd229human GRCh38 chr10: 117,664,803-118,402,207 , GRCh37.p13 chr10: 119,424,314-120,161,719 RAB11FIP2, FAM204A, 6 more genes
    nsv6890475copy number variation1nstd229human GRCh38 chr10: 118,216,756-118,246,002 , GRCh37.p13 chr10: 119,976,268-120,005,514 LINC02944
    nsv6884899copy number variation1nstd229human GRCh38 chr10: 118,227,454-118,244,090 , GRCh37.p13 chr10: 119,986,966-120,003,602 LINC02944
    nsv6620317copy number variation1nstd224human GRCh37 chr10: 119,424,467-120,159,880 , GRCh38.p12 chr10: 117,664,956-118,400,368 RAB11FIP2, FAM204A, 6 more genes
    nsv6314129copy number variation1nstd102humanPathogenic GRCh37 chr10: 117,019,650-125,217,066 , GRCh38.p12 chr10: 115,260,173-123,457,550 PDZD8, MIR3663HG, 122 more genes
    nsv6314085copy number variation1nstd102humanPathogenic GRCh37 chr10: 108,455,687-135,427,143 , GRCh38.p12 chr10: 106,695,929-133,613,639 LOC107984268, DPYSL4, 379 more genes
    nsv6290269copy number variation1nstd102humanUncertain significance GRCh37 chr10: 118,891,670-122,349,064 , GRCh38.p12 chr10: 117,132,159-120,589,552 MCMBP, PDZD8, 54 more genes
    nsv6184700copy number variation1nstd214human GRCh38 chr10: 118,248,307-118,248,390 , GRCh37.p13 chr10: 120,007,819-120,007,902 LINC02944
    nsv6177002copy number variation1nstd214human GRCh38 chr10: 118,248,318-118,248,377 , GRCh37.p13 chr10: 120,007,830-120,007,889 LINC02944
    nsv6168122copy number variation1nstd214human GRCh38 chr10: 118,248,316-118,248,377 , GRCh37.p13 chr10: 120,007,828-120,007,889 LINC02944
    nsv6131937copy number variation1nstd213human GRCh37 chr10: 119,240,000-120,730,001 , GRCh38.p12 chr10: 117,480,489-118,970,489 EMX2, PRLHR, 16 more genes
    nsv6131932copy number variation1nstd213human GRCh37 chr10: 115,960,000-125,870,001 , GRCh38.p12 chr10: 114,200,241-124,109,956 ACADSB, DMBT1, 148 more genes
    nsv6131856copy number variation1nstd213human GRCh37 chr10: 119,980,000-120,050,001 , GRCh38.p12 chr10: 118,220,488-118,290,489 LINC02944
    nsv6131855copy number variation1nstd213human GRCh37 chr10: 119,840,000-120,050,001 , GRCh38.p12 chr10: 118,080,489-118,290,489 CASC2, LINC02944
    nsv6131766copy number variation1nstd213human GRCh37 chr10: 116,010,000-125,870,001 , GRCh38.p12 chr10: 114,250,241-124,109,956 ACADSB, DMBT1, 146 more genes
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv6098176insertion1nstd212human GRCh38 chr10: 118,248,242-118,248,242 , GRCh37.p13 chr10: 120,007,754-120,007,754 LINC02944
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