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 98

    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
    nsv7096148copy number variation2nstd102humanUncertain significance GRCh37 chr2: 24,443,763-29,022,169 , GRCh38.p12 chr2: 24,220,894-28,799,303 LOC105374381, SLC35F6, 122 more genes
    nsv7046929inversion1nstd229human GRCh38 chr2: 27,161,080-28,820,407 , GRCh37.p13 chr2: 27,383,948-29,043,273 LOC100422227, PLB1, 54 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
    nsv6671237copy number variation1nstd229human GRCh38 chr2: 27,575,864-27,575,990 , GRCh37.p13 chr2: 27,798,731-27,798,857 SPATA31H1
    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
    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
    nsv5988834copy number variation1nstd212human GRCh38 chr2: 27,581,568-27,581,638 , GRCh37.p13 chr2: 27,804,435-27,804,505 SPATA31H1, ZNF512
    nsv5976461inversion1nstd209human GRCh38 chr2: 27,448,313-28,588,967 , GRCh37.p13 chr2: 27,671,180-28,811,834 , FOSL2, 31 more genes
    nsv4335876sequence alteration1nstd166human GRCh37.p13 chr2: 20,021,666-53,788,063 , GRCh38.p12 chr2: 19,821,905-53,560,926 , ADCY3, 531 more genes
    nsv4318621inversion1nstd166human GRCh37.p13 chr2: 21,612,232-41,909,281 , GRCh38.p12 chr2: 21,389,360-41,682,141 , CAD, 329 more genes
    nsv4055317copy number variation1nstd166human GRCh37.p13 chr2: 27,797,503-27,797,599 , GRCh38.p12 chr2: 27,574,636-27,574,732 SPATA31H1
    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