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 339

    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
    nsv7098355copy number variation1nstd102humanUncertain significance GRCh37 chrX: 153,760,215-153,764,413 , GRCh38.p12 chrX: 154,532,000-154,536,198 G6PD
    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
    nsv7098245copy number variation3nstd102humanUncertain significance GRCh37 chrX: 153,640,181-153,775,961 , GRCh38.p12 chrX: 154,411,844-154,547,746 TAFAZZIN, FAM3A, 13 more genes
    nsv7098009copy number variation1nstd102humanUncertain significance GRCh37 chrX: 153,762,230-153,775,961 , GRCh38.p12 chrX: 154,534,015-154,547,746 G6PD, IKBKG
    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
    nsv7079937copy number variation1nstd229human GRCh38 chrX: 154,537,059-154,537,134 , GRCh37.p13 chrX: 153,765,274-153,765,349 , GRCh37.p13 chrX|NW_003871103.3: 1,971,038-1,971,113 G6PD
    nsv7079936copy number variation1nstd229human GRCh38 chrX: 154,527,301-154,553,500 , GRCh37.p13 chrX|NW_003871103.3: 1,961,280-1,987,479 , GRCh37.p13 chrX: 153,755,515-153,781,715 IKBKG, G6PD
    nsv7079935copy number variation1nstd229human GRCh38 chrX: 154,519,503-154,533,224 , GRCh37.p13 chrX|NW_003871103.3: 1,953,482-1,967,203 , GRCh37.p13 chrX: 153,747,823-153,761,439 G6PD
    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
    nsv7079918copy number variation1nstd229human GRCh38 chrX: 154,461,119-154,608,559 , GRCh37.p13 chrX: 153,689,459-153,836,812 , GRCh37.p13 chrX|NW_003871103.3: 1,895,098-2,042,538 UBL4A, FAM3A, 9 more genes
    nsv7079912copy number variation1nstd229human GRCh38 chrX: 154,457,238-154,596,819 , GRCh37.p13 chrX: 153,685,578-153,825,080 , GRCh37.p13 chrX|NW_003871103.3: 1,891,217-2,030,798 CTAG1A, PLXNA3, 9 more genes
    nsv7079883copy number variation1nstd229human GRCh38 chrX: 154,333,501-154,534,400 , GRCh37.p13 chrX|NW_003871103.3: 1,767,480-1,968,379 , GRCh37.p13 chrX: 153,561,851-153,762,615 G6PD, FLNA, 17 more genes
    nsv7079878copy number variation1nstd229human GRCh38 chrX: 154,309,633-154,536,356 , GRCh37.p13 chrX|NW_003871103.3: 1,743,612-1,970,335 , GRCh37.p13 chrX: 153,537,985-153,764,571 SNORA70, LOC105373386, 18 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
    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
    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