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 350

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054091inversion1nstd229human GRCh38 chr3: 193,070,088-193,184,801 , GRCh37.p13 chr3: 192,787,877-192,902,590 VEZF1P1
    nsv7049138inversion1nstd229human GRCh38 chr3: 193,070,073-193,175,792 , GRCh37.p13 chr3: 192,787,862-192,893,581 VEZF1P1
    nsv7039647inversion1nstd229human GRCh38 chr3: 192,804,119-193,189,826 , GRCh37.p13 chr3: 192,521,908-192,907,615 MB21D2, VEZF1P1
    nsv7039556inversion1nstd229human GRCh38 chr3: 192,908,987-193,401,493 , GRCh37.p13 chr3: 192,626,776-193,119,282 VEZF1P1, ATP13A5-AS1, 6 more genes
    nsv6734467copy number variation1nstd229human GRCh38 chr3: 193,076,188-193,196,854 , GRCh37.p13 chr3: 192,793,977-192,914,643 VEZF1P1
    nsv6731714copy number variation1nstd229human GRCh38 chr3: 192,378,501-195,488,100 , GRCh37.p13 chr3: 192,096,290-195,214,903 LSG1, MB21D2, 61 more genes
    nsv6729518copy number variation1nstd229human GRCh38 chr3: 192,733,365-193,370,673 , GRCh37.p13 chr3: 192,451,154-193,088,462 ATP13A5, ATP13A5-AS1, 6 more genes
    nsv6726306copy number variation1nstd229human GRCh38 chr3: 193,149,801-193,151,900 , GRCh37.p13 chr3: 192,867,590-192,869,689 VEZF1P1
    nsv6634371copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 171,549,421-198,022,430 , GRCh38.p12 chr3: 171,831,631-198,235,559 ACTL6A, AHSG, 466 more genes
    nsv6315437copy number variation1nstd102humanPathogenic GRCh37 chr3: 183,498,520-197,851,986 , GRCh38.p12 chr3: 183,780,732-198,125,115 LOC105374291, GP5, 315 more genes
    nsv6313527copy number variation1nstd102humanUncertain significance GRCh37 chr3: 192,607,378-194,745,252 , GRCh38.p12 chr3: 192,889,589-195,024,523 LINC02036, HES1, 48 more genes
    nsv6290259copy number variation1nstd102humanPathogenic GRCh37 chr3: 189,608,636-197,532,175 , GRCh38.p12 chr3: 189,890,847-197,805,304 LINC01972, LINC02026, 174 more genes
    nsv6290248copy number variation1nstd102humanPathogenic GRCh37 chr3: 191,866,466-197,842,171 , GRCh38.p12 chr3: 192,148,677-198,115,300 PIGZ, LOC107986173, 156 more genes
    nsv6134833copy number variation1nstd213human GRCh37 chr3: 186,910,000-193,810,001 , GRCh38.p12 chr3: 187,192,212-194,092,212 BCL6, LPP, 85 more genes
    nsv5992682copy number variation1nstd212human GRCh38 chr3: 193,157,543-193,167,617 , GRCh37.p13 chr3: 192,875,332-192,885,406 VEZF1P1
    nsv5905289copy number variation1nstd209human GRCh38 chr3: 193,157,540-193,167,615 , GRCh37.p13 chr3: 192,875,329-192,885,404 VEZF1P1
    nsv5835180copy number variation1nstd209human GRCh38 chr3: 193,157,551-193,163,050 , GRCh37.p13 chr3: 192,875,340-192,880,839 VEZF1P1
    nsv5687197mobile element insertion2nstd211human GRCh38 chr3: 193,152,092-193,152,092 , GRCh37.p13 chr3: 192,869,881-192,869,881 VEZF1P1
    nsv5582351copy number variation1nstd207human GRCh38 chr3: 193,157,540-193,167,615 , GRCh37.p13 chr3: 192,875,329-192,885,404 VEZF1P1
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 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