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 335

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137735copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,194,251-153,623,000 , GRCh38.p12 chrX: 153,928,798-154,394,658 EMD, MIR3202-1, 20 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
    nsv5980455copy number variation1nstd102humanPathogenic GRCh38 chrX: 153,884,414-154,363,935 , GRCh37.p13 chrX|NW_003871103.3: 1,318,396-1,797,914 , GRCh37.p13 chrX: 153,149,868-153,592,303 MIR3202-1, FLNA, 23 more genes
    nsv5673835copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,128,098-153,498,669 , GRCh38.p12 chrX: 153,862,643-154,233,200 OPN1MW, IRAK1, 18 more genes
    nsv5564517copy number variation1nstd102humanPathogenic GRCh38 chrX: 153,858,452-154,332,213 , GRCh37.p13 chrX|NW_003871103.3: 1,292,435-1,766,192 , GRCh37.p13 chrX: 153,123,907-153,560,563 OPN1MW2, ARHGAP4, 22 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
    nsv4894184copy number variation1nstd200human GRCh38 chrX: 153,947,848-153,947,925 , GRCh37.p13 chrX|NW_003871103.3: 1,381,827-1,381,904 , GRCh37.p13 chrX: 153,213,299-153,213,376 HCFC1
    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
    nsv4728292copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,135,257-153,594,096 , GRCh38.p12 chrX: 153,869,802-154,365,728 NAA10, OPN1MW3, 23 more genes
    nsv4728215copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,113,943-153,624,215 , GRCh38.p12 chrX: 153,848,488-154,395,874 ARHGAP4, L1CAM, 24 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
    nsv4681289copy number variation1nstd102humanPathogenic GRCh37 chrX: 152,954,010-153,363,142 , GRCh38.p12 chrX: 153,688,555-154,097,685 NAA10, RENBP, 22 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
    nsv4674564copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 153,023,149-153,345,755 , GRCh38.p12 chrX: 153,757,695-154,080,303 ARHGAP4, AVPR2, 19 more genes
    nsv4674212copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,029,046-153,567,369 , GRCh38.p12 chrX: 153,763,591-154,339,019 TEX28P2, LOC105373386, 29 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