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 274

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137666copy number variation1nstd102humanPathogenic GRCh37 chrX: 91,829,757-113,050,225 , GRCh38.p12 chrX: 92,574,758-113,806,943 TCEAL8, MTND5P26, 272 more genes
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5665884copy number variation1nstd207human GRCh38 chrX: 107,274,225-107,274,288 , GRCh37.p13 chrX: 106,517,455-106,517,518 MYCLP1
    nsv5059979copy number variation1nstd102humanPathogenic GRCh37 chrX: 56,469,080-155,233,731 , GRCh38.p12 chrX: 56,442,647-156,004,066 VDAC1P1, LOC105373299, 1364 more genes
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 more genes
    nsv4905842copy number variation1nstd200human GRCh38 chrX: 107,064,984-107,532,736 , GRCh37.p13 chrX: 106,308,214-106,775,966 NUP62CL, DNAAF6, 7 more genes
    nsv4782241copy number variation1nstd200human GRCh37 chrX: 106,308,214-106,775,966 , GRCh38.p12 chrX: 107,064,984-107,532,736 MYCLP1, FRMPD3-AS1, 7 more genes
    nsv4769250copy number variation1nstd201human GRCh37 chrX: 96,096,220-155,208,244 , GRCh38.p12 chrX: 96,841,221-155,978,579 , AGTR2, 959 more genes
    nsv4769249copy number variation1nstd201human GRCh37 chrX: 61,728,816-155,233,846 , GRCh38.p12 chrX: 62,509,346-156,004,181 , ABCB7, 1364 more genes
    nsv4728601copy number variation1nstd102humanPathogenic GRCh37 chrX: 77,514,079-127,770,854 , GRCh38.p12 chrX: 78,258,582-128,636,876 PHB1P10, SNORA35, 565 more genes
    nsv4728533copy number variation1nstd102humanPathogenic GRCh37 chrX: 94,264,404-155,233,731 , GRCh38.p12 chrX: 95,009,405-156,004,066 CT45A10, MIR224, 968 more genes
    nsv4728499copy number variation1nstd102humanPathogenic GRCh37 chrX: 55,507,789-155,198,481 , GRCh38.p12 chrX: 55,481,356-155,968,816 GABRE, RN7SL325P, 1371 more genes
    nsv4728258copy number variation1nstd102humanUncertain significance GRCh37 chrX: 106,479,615-107,575,960 , GRCh38.p12 chrX: 107,236,385-108,332,730 COL4A6, ATG4A, 16 more genes
    nsv4674753copy number variation1nstd102humanPathogenic GRCh37 chrX: 78,444,738-155,233,731 , GRCh38.p12 chrX: 79,189,241-156,004,066 PAK3, ZCCHC12, 1069 more genes
    nsv4674080copy number variation1nstd102humanPathogenic GRCh37 chrX: 84,387,417-155,233,731 , GRCh38.p12 chrX: 85,132,411-156,004,066 CSTF2, GPR119, 1029 more genes
    nsv4674000copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 105,973,323-110,619,655 , GRCh38.p12 chrX: 106,730,093-111,376,427 CAPN6, COL4A5, 53 more genes
    nsv4578586copy number variation1nstd102humanPathogenic GRCh37 chrX: 101,029,649-106,702,784 , GRCh38.p12 chrX: 101,774,676-107,459,554 GLRA4, TMSB15B, 115 more genes
    nsv4453035copy number variation1nstd102humanUncertain significance GRCh37 chrX: 106,423,942-106,937,868 , GRCh38.p12 chrX: 107,180,712-107,694,638 FRMPD3-AS1, DNAAF6, 6 more genes
    nsv4452492copy number variation1nstd102humanPathogenic GRCh37 chrX: 58,455,352-155,233,731 , GRCh38.p12 chrX: 58,428,919-156,004,066 RNU6-122P, LOC100421910, 1347 more genes
    nsv4452442copy number variation1nstd102humanPathogenic GRCh37 chrX: 92,814,516-155,233,731 , GRCh38.p12 chrX: 93,559,517-156,004,066 TEX13D, CT45A5, 978 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