U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 104

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5723929mobile element insertion1nstd211human GRCh38 chr10: 100,535,337-100,535,337 , GRCh37.p13 chr10: 102,295,094-102,295,094 HIF1AN
    nsv5711874mobile element insertion1nstd211human GRCh38 chr10: 100,542,869-100,542,869 , GRCh37.p13 chr10: 102,302,626-102,302,626 HIF1AN
    nsv5705664mobile element insertion2nstd211human GRCh38 chr10: 100,554,008-100,554,008 , GRCh37.p13 chr10: 102,313,765-102,313,765 HIF1AN
    nsv5554654mobile element insertion1nstd206human GRCh38 chr10: 100,535,353-100,535,388 , GRCh37.p13 chr10: 102,295,110-102,295,145 HIF1AN
    nsv5398235mobile element insertion1nstd206human GRCh38 chr10: 100,554,008-100,554,059 , GRCh37.p13 chr10: 102,313,765-102,313,816 HIF1AN
    nsv5121935mobile element insertion1nstd203human GRCh38 chr10: 100,553,993-100,554,008 , GRCh37.p13 chr10: 102,313,750-102,313,765 HIF1AN
    nsv4674975copy number variation1nstd102humanUncertain significance GRCh37 chr10: 101,932,457-102,392,841 , GRCh38.p12 chr10: 100,172,700-100,633,084 NDUFB8, SNORA12, 12 more genes
    nsv4543209insertion1nstd166human GRCh37.p13 chr10: 102,297,584-102,297,584 , GRCh38.p12 chr10: 100,537,827-100,537,827 HIF1AN
    nsv4488447mobile element insertion1nstd166human GRCh37.p13 chr10: 102,313,750-102,313,750 , GRCh38.p12 chr10: 100,553,993-100,553,993 HIF1AN
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4325673inversion1nstd166human GRCh37.p13 chr10: 92,228,734-107,785,320 , GRCh38.p12 chr10: 90,468,977-106,025,562 , COX15, 323 more genes
    nsv3923769copy number variation1nstd102humanPathogenic GRCh38 chr10: 100,194,215-132,432,797 , GRCh37 chr10: 101,953,972-134,246,301 , NCBI36 chr10: 101,943,962-134,096,291 LOC105378493, LINC02627, 477 more genes
    nsv3920295copy number variation1nstd102humanPathogenic NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422 EIF2S2P3, CYP17A1-AS1, 895 more genes
    nsv3911437copy number variation1nstd102humanPathogenic GRCh38 chr10: 93,181,201-101,356,779 , NCBI36 chr10: 94,930,948-103,106,526 , GRCh37 chr10: 94,940,958-103,116,536 SLF2, CUTC, 171 more genes
    nsv3911005copy number variation1nstd102humanUncertain significance GRCh37 chr10: 101,146,389-102,407,978 , NCBI36 chr10: 101,136,379-102,397,968 , GRCh38 chr10: 99,386,632-100,648,221 NDUFB8, MTATP8P4, 32 more genes
    nsv3909942copy number variation1nstd102humanPathogenic GRCh37 chr10: 96,872,364-118,383,651 , GRCh38 chr10: 95,112,607-116,776,637 , NCBI36 chr10: 96,862,354-118,526,138 LOC102723665, SFR1, 360 more genes
    nsv3907664copy number variation1nstd102humandrug response GRCh37 chr10: 42,347,406-135,534,747 , GRCh38.p12 chr10: 42,101,241-133,787,422 SHOC2, FAM245B, 1487 more genes
    nsv3906389copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996 LOC100419870, LOC102724439, 2105 more genes
    nsv3905489copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,283,493-135,427,143 , GRCh38.p12 chr10: 91,523,736-133,613,639 LOC105378476, SMC3, 688 more genes
    nsv3902271copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639 ANXA11, EDRF1-DT, 2085 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center