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 298

    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
    nsv6112666copy number variation1nstd102humanPathogenic GRCh37 chrX: 139,484,271-149,442,579 , GRCh38.p12 chrX: 140,402,106-150,274,366 MIR508, SPANXN1, 121 more genes
    nsv5557365sequence alteration1nstd206human GRCh37.p13 chrX|NW_004070890.2: 5,059,217-5,469,910 , GRCh38 chrX: 149,534,819-149,945,512 , GRCh37.p13 chrX: 148,616,351-149,113,730 MAGEA9, HSFX2, 19 more genes
    nsv5428659copy number variation1nstd206human GRCh38 chrX: 149,748,700-149,917,606 , GRCh37.p13 chrX|NW_004070890.2: 5,273,098-5,442,004 , GRCh37.p13 chrX: 148,830,361-149,085,824 LINC00850, MAGEA8, 8 more genes
    nsv5428135copy number variation1nstd206human GRCh37.p13 chrX|NW_004070890.2: 5,178,004-5,308,004 , GRCh38 chrX: 149,653,606-149,783,606 , GRCh37.p13 chrX: 148,735,274-148,865,268 MAGEA9, MAGEA11, 4 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
    nsv4782431copy number variation1nstd200human GRCh37 chrX: 148,769,378-149,527,672 , GRCh38.p12 chrX: 149,687,712-150,359,419 MAGEA7P, LOC643015, 15 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
    nsv4752636inversion1nstd199human GRCh37 chrX: 148,655,522-148,877,186 , GRCh38.p12 chrX: 149,573,866-149,795,524 MAGEA9, MAGEA11, 8 more genes
    nsv4730128inversion50nstd198human GRCh37.p13 chrX: 148,659,876-148,870,140 , GRCh38 chrX: 149,578,220-149,788,478 , GRCh37.p13 chrX|NW_004070890.2: 5,102,618-5,312,876 MAGEA9, MAGEA11, 8 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
    nsv4728473copy number variation1nstd102humanLikely benign GRCh37 chrX: 148,448,248-148,855,992 , GRCh38.p12 chrX: 149,366,718-149,774,334 MAGEA11, TMEM185A, 14 more genes
    nsv4728189copy number variation1nstd102humanLikely benign GRCh37 chrX: 148,538,098-148,855,992 , GRCh38.p12 chrX: 149,456,567-149,774,334 TMEM185AP1, LOC100420334, 14 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
    nsv4679893copy number variation1nstd189human GRCh37.p13 chrX: 113,759,648-150,222,670 , GRCh38.p12 chrX: 114,525,195-151,054,198 , AGTR2, 532 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
    nsv4674523copy number variation1nstd102humanLikely benign GRCh37 chrX: 148,392,776-148,855,992 , GRCh38.p12 chrX: 149,311,246-149,774,334 LOC100420322, HSFX3, 14 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
    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