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 302

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    nsv7079941copy number variation1nstd229human GRCh38 chrX: 154,611,162-154,753,512 , GRCh37.p13 chrX|NW_003871103.3: 2,045,141-2,187,491 , GRCh37.p13 chrX: 153,839,415-153,981,787 OR3B1P, IKBKGP1, 6 more genes
    nsv7079933copy number variation1nstd229human GRCh38 chrX: 154,505,501-154,724,500 , GRCh37.p13 chrX: 153,733,832-153,952,775 , GRCh37.p13 chrX|NW_003871103.3: 1,939,480-2,158,479 FAM223B, CTAG1A, 12 more genes
    nsv7079921copy number variation1nstd229human GRCh38 chrX: 154,494,011-154,710,575 , GRCh37.p13 chrX|NW_003871103.3: 1,927,990-2,144,554 , GRCh37.p13 chrX: 153,722,357-153,938,850 G6PD, FAM223B, 13 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
    nsv7050020inversion1nstd229human GRCh38 chrX: 154,606,471-155,052,434 , GRCh37.p13 chrX: 153,834,724-154,280,709 , GRCh37.p13 chrX|NW_003871103.3: 2,040,450-2,486,413 EEF1A1P31, HMGN1P37, 20 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
    nsv7042456inversion1nstd229human GRCh38 chrX: 154,553,086-155,008,344 , GRCh37.p13 chrX|NW_003871103.3: 1,987,065-2,442,323 , GRCh37.p13 chrX: 153,781,301-154,236,619 F8, OR3B1P, 23 more genes
    nsv6637094copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,613,883-155,233,731 , GRCh38.p12 chrX: 154,385,523-156,004,066 FAM3A, TAFAZZIN, 65 more genes
    nsv6637076copy number variation1nstd102humanUncertain significance GRCh37 chrX: 153,868,487-154,071,392 , GRCh38.p12 chrX: 154,640,212-154,843,117 SNORA36A, GAB3, 11 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
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6634237copy number variation1nstd224human GRCh37 chrX: 149,422,813-154,913,173 , GRCh38.p12 chrX: 150,254,602-155,683,512 ABCD1, FLNA, 182 more genes
    nsv6315439copy number variation2nstd102humanPathogenic GRCh37 chrX: 152,372,767-155,233,731 , GRCh38.p12 chrX: 153,106,941-156,004,066 SNORA36A, VBP1, 126 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