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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148145copy number variation1nstd102humanPathogenic GRCh38 chrX: 154,375,606-154,392,000 , GRCh37.p13 chrX|NW_003871103.3: 1,809,585-1,825,979 , GRCh37.p13 chrX: 153,603,974-153,620,342 EMD
    nsv7148061copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,217,915-153,618,382 , GRCh38.p12 chrX: 153,952,464-154,390,022 MIR3202-1, LOC105373386, 18 more genes
    nsv7138382insertion1nstd232human GRCh37.p13 chrX: 153,608,729-153,608,729 , GRCh38.p12 chrX: 154,380,369-154,380,369 EMD
    nsv7137089copy number variation1nstd102humannot provided GRCh37 chrX: 153,566,798-153,748,208 , GRCh38.p12 chrX: 154,338,448-154,519,994 SLC10A3, FLNA, 16 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098869copy number variation1nstd102humanPathogenic GRCh37 chrX: 139,586,015-154,774,957 , GRCh38.p12 chrX: 140,503,850-155,545,296 MAGEA6, LOC101928832, 303 more genes
    nsv7098599copy number variation1nstd102humanUncertain significance GRCh37 chrX: 153,001,546-154,563,736 , GRCh38.p12 chrX: 153,736,092-155,334,427 TAFAZZIN, LOC105373386, 82 more genes
    nsv7098354copy number variation1nstd102humanUncertain significance GRCh37 chrX: 153,585,782-153,775,961 , GRCh38.p12 chrX: 154,357,414-154,547,746 UBL4A, GDI1, 17 more genes
    nsv7098350copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,195,397-153,642,547 , GRCh38.p12 chrX: 153,929,944-154,414,210 TKTL1, IRAK1, 24 more genes
    nsv7098243copy number variation1nstd102humanUncertain significance GRCh37 chrX: 153,586,547-153,609,557 , GRCh38.p12 chrX: 154,358,179-154,381,197 FLNA, EMD
    nsv7098007copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,607,393-153,608,624 , GRCh38.p12 chrX: 154,379,033-154,380,264 EMD
    nsv7098006copy number variation1nstd102humanUncertain significance GRCh37 chrX: 153,357,622-153,664,237 , GRCh38.p12 chrX: 154,092,164-154,435,891 EMD, FLNA, 18 more genes
    nsv7098002copy number variation1nstd102humanUncertain significance GRCh37 chrX: 153,128,118-153,664,237 , GRCh38.p12 chrX: 153,862,663-154,435,891 OPN1MW, TEX28, 31 more genes
    nsv7097996copy number variation6nstd102humanPathogenic GRCh37 chrX: 152,014,869-155,171,615 , GRCh38.p12 chrX: 152,846,325-155,941,951 PHF10P1, ZNF185, 132 more genes
    nsv7097995copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chrX: 152,014,869-154,563,736 , GRCh38.p12 chrX: 152,846,325-155,334,427 RN7SL697P, CYCSP45, 118 more genes
    nsv7079897copy number variation1nstd229human GRCh38 chrX: 154,378,101-154,402,400 , GRCh37.p13 chrX|NW_003871103.3: 1,812,080-1,836,379 , GRCh37.p13 chrX: 153,606,461-153,630,741 SNORA70, RPL10, 2 more genes
    nsv7079896copy number variation1nstd229human GRCh38 chrX: 154,376,201-154,407,100 , GRCh37.p13 chrX: 153,604,561-153,635,441 , GRCh37.p13 chrX|NW_003871103.3: 1,810,180-1,841,079 EMD, DNASE1L1, 2 more genes
    nsv7079893copy number variation1nstd229human GRCh38 chrX: 154,362,101-154,505,500 , GRCh37.p13 chrX|NW_003871103.3: 1,796,080-1,939,479 , GRCh37.p13 chrX: 153,590,469-153,733,831 PLXNA3, ATP6AP1-DT, 15 more genes
    nsv7079892copy number variation1nstd229human GRCh38 chrX: 154,360,201-154,402,400 , GRCh37.p13 chrX: 153,588,569-153,630,741 , GRCh37.p13 chrX|NW_003871103.3: 1,794,180-1,836,379 RPL10, SNORA70, 3 more genes
    nsv7079891copy number variation1nstd229human GRCh38 chrX: 154,359,801-154,444,500 , GRCh37.p13 chrX: 153,588,169-153,672,848 , GRCh37.p13 chrX|NW_003871103.3: 1,793,780-1,878,479 ATP6AP1, FAM50A, 8 more genes
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