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 114

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6833828copy number variation1nstd229human GRCh38 chr7: 40,448,601-40,578,600 , GRCh37.p13 chr7: 40,488,200-40,618,199 SUGCT-AS1, LOC105375244, 1 more genes
    nsv6831661copy number variation1nstd229human GRCh38 chr7: 40,541,042-40,557,218 , GRCh37.p13 chr7: 40,580,641-40,596,817 SUGCT, SUGCT-AS1
    nsv6831631copy number variation1nstd229human GRCh38 chr7: 40,524,302-40,673,735 , GRCh37.p13 chr7: 40,563,901-40,713,334 SUGCT, SUGCT-AS1, 1 more genes
    nsv6830646copy number variation1nstd229human GRCh38 chr7: 39,656,501-41,139,000 , GRCh37.p13 chr7: 39,696,100-41,178,598 RALA, LOC105375242, 22 more genes
    nsv6829098copy number variation1nstd229human GRCh38 chr7: 40,533,926-40,680,952 , GRCh37.p13 chr7: 40,573,525-40,720,551 SUGCT-AS1, LOC105375244, 1 more genes
    nsv6828397copy number variation1nstd229human GRCh38 chr7: 40,405,584-40,656,157 , GRCh37.p13 chr7: 40,445,183-40,695,756 SUGCT, SUGCT-AS1, 1 more genes
    nsv6827922copy number variation1nstd229human GRCh38 chr7: 40,507,175-40,595,641 , GRCh37.p13 chr7: 40,546,774-40,635,240 SUGCT-AS1, LOC105375244, 1 more genes
    nsv6826002copy number variation1nstd229human GRCh38 chr7: 40,436,195-40,563,921 , GRCh37.p13 chr7: 40,475,794-40,603,520 SUGCT-AS1, LOC105375244, 1 more genes
    nsv6823262copy number variation1nstd229human GRCh38 chr7: 40,543,898-40,554,680 , GRCh37.p13 chr7: 40,583,497-40,594,279 SUGCT-AS1, SUGCT
    nsv6822749copy number variation1nstd229human GRCh38 chr7: 40,538,131-40,539,506 , GRCh37.p13 chr7: 40,577,730-40,579,105 SUGCT-AS1, SUGCT
    nsv6822106copy number variation1nstd229human GRCh38 chr7: 40,259,092-40,727,988 , GRCh37.p13 chr7: 40,298,691-40,767,587 LOC105375244, LOC105375243, 3 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6601799copy number variation1nstd223human GRCh38 chr7: 40,400,687-40,584,267 , GRCh37.p13 chr7: 40,440,286-40,623,866 LOC105375244, SUGCT-AS1, 1 more genes
    nsv6574607inversion1nstd223human GRCh38 chr7: 35,958,610-45,735,691 , GRCh37.p13 chr7: 35,998,220-45,775,290 RPS17P13, LOC105375252, 182 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6312346copy number variation1nstd102humanPathogenic GRCh37 chr7: 39,726,267-42,262,852 , GRCh38.p12 chr7: 39,686,668-42,223,253 HMGN2P30, GLI3, 31 more genes
    nsv6136995copy number variation1nstd213human GRCh37 chr7: 39,040,000-48,190,001 , GRCh38.p12 chr7: 39,000,400-48,150,404 ADCY1, AEBP1, 161 more genes
    nsv6135992copy number variation1nstd213human GRCh37 chr7: 39,290,000-48,200,001 , GRCh38.p12 chr7: 39,250,401-48,160,404 PSMA2, RALA, 160 more genes
    nsv6135765copy number variation1nstd213human GRCh37 chr7: 40,520,000-41,510,001 , GRCh38.p12 chr7: 40,480,401-41,470,403 LOC105375243, LOC105375246, 9 more genes
    nsv6135764copy number variation1nstd213human GRCh37 chr7: 40,060,000-40,590,001 , GRCh38.p12 chr7: 40,020,401-40,550,402 CDK13, SUGCT, 5 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