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 278

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5880632copy number variation1nstd209human GRCh38 chrX: 153,595,674-153,595,839 , GRCh37.p13 chrX: 152,861,132-152,861,297 , GRCh37.p13 chrX|NW_003871103.3: 1,029,657-1,029,822 CCNQ
    nsv5424612copy number variation1nstd206human GRCh38 chrX: 153,598,348-153,602,178 , GRCh37.p13 chrX|NW_003871103.3: 1,032,331-1,036,161 , GRCh37.p13 chrX: 152,863,806-152,867,633 LOC105373383, CCNQ
    nsv5200296copy number variation1nstd102humanPathogenic GRCh37 chrX: 152,649,825-152,988,014 , GRCh38.p12 chrX: 153,384,367-153,722,559 CCNQ, SLC6A8, 17 more genes
    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
    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
    nsv4728727copy number variation1nstd102humanUncertain significance GRCh37 chrX: 152,631,130-153,240,286 , GRCh38.p12 chrX: 153,365,672-153,974,835 ARHGAP4, BCAP31, 34 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
    nsv4685620copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 122,132,166-155,097,214 , GRCh38.p12 chrX: 122,998,313-155,867,551 ABCD1, AMD1P2, 560 more genes
    nsv4674760copy number variation1nstd102humanPathogenic GRCh37 chrX: 152,516,781-153,368,573 , GRCh38.p12 chrX: 153,251,356-154,103,121 RENBP, TMEM187, 44 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
    nsv4578241copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 122,757,437-155,208,244 , GRCh38.p12 chrX: 123,623,586-155,978,579 ABCD1, AMD1P2, 557 more genes
    nsv4454214copy number variation1nstd102humanPathogenic GRCh37 chrX: 122,924,044-155,233,731 , GRCh38.p12 chrX: 123,790,194-156,004,066 LOC107985666, FLNA, 555 more genes
    nsv4453829copy number variation1nstd102humanUncertain significance GRCh37 chrX: 152,405,258-152,942,804 , GRCh38.p12 chrX: 153,250,227-153,677,349 TREX2, ZFP92, 20 more genes
    nsv4452773copy number variation1nstd102humanUncertain significance GRCh37 chrX: 152,765,599-152,970,126 , GRCh38.p12 chrX: 153,500,141-153,704,671 ATP2B3, LOC105373383, 10 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