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Items: 1 to 20 of 377

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7148059copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,247,464-153,522,710 , GRCh38.p12 chrX: 153,982,013-154,294,356 TEX28, OPN1MW, 11 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
    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
    nsv7098237copy number variation3nstd102humanUncertain significance GRCh37 chrX: 153,195,397-153,583,460 , GRCh38.p12 chrX: 153,929,944-154,355,092 OPN1MW2, TEX28, 19 more genes
    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
    nsv7057928inversion1nstd229human GRCh38 chrX: 152,528,769-155,098,506 , GRCh37.p13 chrX: 151,734,490-154,326,781 , GRCh37.p13 chrX|NW_003871103.3: 1-2,532,485 F8, ATP6AP1, 128 more genes
    nsv7051950inversion1nstd229human GRCh38 chrX: 153,712,302-154,514,525 , GRCh37.p13 chrX: 152,977,757-153,742,849 , GRCh37.p13 chrX|NW_003871103.3: 1,146,285-1,948,504 MIR3202-1, LAGE3, 48 more genes
    nsv7047108inversion1nstd229human GRCh38 chrX: 153,824,232-154,611,904 , GRCh37.p13 chrX: 153,089,687-153,840,157 , GRCh37.p13 chrX|NW_003871103.3: 1,258,215-2,045,883 HCFC1, SNORA70, 46 more genes
    nsv7046320inversion1nstd229human GRCh38 chrX: 152,800,888-155,032,704 , GRCh37.p13 chrX|NW_003871103.3: 234,871-2,466,683 , GRCh37.p13 chrX: 151,969,427-154,260,979 FUNDC2, PNCK, 111 more genes
    nsv7046188inversion1nstd229human GRCh38 chrX: 152,545,731-155,311,806 , GRCh37.p13 chrX: 151,734,490-154,541,118 , GRCh37.p13 chrX|NW_003871103.3: 1-2,745,785 TEX28, SSR4, 133 more genes
    nsv6636807copy number variation1nstd102humanUncertain significance GRCh37 chrX: 153,421,785-153,624,604 , GRCh38.p12 chrX: 154,156,310-154,396,263 TEX28P3, OPN1LW, 11 more genes
    nsv6636778copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,282,944-153,681,801 , GRCh38.p12 chrX: 154,017,493-154,453,453 TAFAZZIN, SNORA70, 22 more genes
    nsv6636407copy number variation1nstd102humanPathogenic GRCh37 chrX: 124,749,464-155,233,731 , GRCh38.p12 chrX: 125,615,468-156,004,066 RN7SKP31, LOC728470, 539 more genes
    nsv6634391copy number variation1nstd102humanPathogenic GRCh37 chrX: 142,401,540-155,233,731 , GRCh38.p12 chrX: 143,313,746-156,004,066 CSAG4, LOC112268308, 279 more genes
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