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 117

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096625copy number variation1nstd102humanUncertain significance GRCh37 chr2: 24,443,763-30,143,525 , GRCh38.p12 chr2: 24,220,894-29,920,659 LOC105374381, POMC, 136 more genes
    nsv7045006inversion1nstd229human GRCh38 chr2: 28,892,565-29,348,187 , GRCh37.p13 chr2: 29,115,431-29,571,053 SNORD92, LOC105374386, 8 more genes
    nsv7042984inversion1nstd229human GRCh38 chr2: 26,886,657-32,818,427 , GRCh37.p13 chr2: 27,109,525-33,043,494 CLIP4, LOC102723594, 118 more genes
    nsv6672785copy number variation1nstd229human GRCh38 chr2: 24,384,939-32,866,867 , GRCh37.p13 chr2: 24,607,808-33,091,934 CENPO, TOGARAM2, 170 more genes
    nsv6665994copy number variation1nstd229human GRCh38 chr2: 28,736,946-29,025,229 , GRCh37.p13 chr2: 28,959,812-29,248,095 TOGARAM2, PPP1CB-DT, 7 more genes
    nsv6658568copy number variation1nstd229human GRCh38 chr2: 28,879,126-29,482,143 , GRCh37.p13 chr2: 29,101,992-29,705,009 LOC101929386, SNORD92, 9 more genes
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 LOC105374455, RN7SL674P, 504 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6546927inversion1nstd223human GRCh38 chr2: 26,476,473-32,916,584 , GRCh37.p13 chr2: 26,699,341-33,141,651 LOC105374453, LCLAT1, 129 more genes
    nsv6543735inversion1nstd223human GRCh38 chr2: 24,403,241-32,916,237 , GRCh37.p13 chr2: 24,626,110-33,141,304 LOC105374334, LOC107985861, 172 more genes
    nsv6538559inversion1nstd223human GRCh38 chr2: 25,762,333-32,867,002 , GRCh37.p13 chr2: 25,985,202-33,092,069 MIR558, PCARE, 148 more genes
    nsv6344534copy number variation1nstd223human GRCh38 chr2: 24,831,925-32,916,230 , GRCh37.p13 chr2: 25,054,794-33,141,297 LOC102723594, DNAJC5G, 165 more genes
    nsv6340057copy number variation1nstd223human GRCh38 chr2: 28,926,552-28,927,566 , GRCh37.p13 chr2: 29,149,418-29,150,432 SNORD53, SNORD53B, 1 more genes
    nsv6336585copy number variation1nstd223human GRCh38 chr2: 28,879,126-29,482,141 , GRCh37.p13 chr2: 29,101,992-29,705,007 SNORD53, LOC105374386, 9 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6137788copy number variation1nstd102humanPathogenic GRCh37 chr2: 24,601,818-43,466,284 , GRCh38.p12 chr2: 24,378,949-43,239,145 GTF3C2-AS1, MAPRE3-AS1, 316 more genes
    nsv6112680copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 24,881,528-43,460,021 , GRCh38.p12 chr2: 24,658,659-43,232,882 ADCY3, ALK, 314 more genes
    nsv5564430copy number variation1nstd102humanUncertain significance GRCh37 chr2: 29,119,585-29,450,548 , GRCh38.p12 chr2: 28,896,719-29,227,682 SNORD92, LOC105374386, 7 more genes
    nsv5564185copy number variation1nstd102humanUncertain significance GRCh37 chr2: 29,119,585-30,143,525 , GRCh38.p12 chr2: 28,896,719-29,920,659 WDR43, CLIP4, 10 more genes
    nsv4674305copy number variation1nstd102humanUncertain significance GRCh37 chr2: 28,387,514-29,616,031 , GRCh38.p12 chr2: 28,164,647-29,393,165 BABAM2, FOSL2, 27 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center