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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7044096inversion1nstd229human GRCh38 chr2: 5,896,641-9,131,731 , GRCh37.p13 chr2: 6,036,773-9,271,860 LOC105373407, LOC107985847, 48 more genes
    nsv6677695copy number variation1nstd229human GRCh38 chr2: 6,154,901-7,419,900 , GRCh37.p13 chr2: 6,295,033-7,560,031 NRIR, LINC00487, 20 more genes
    nsv6675091copy number variation1nstd229human GRCh38 chr2: 6,898,030-6,902,051 , GRCh37.p13 chr2: 7,038,161-7,042,182 RSAD2
    nsv6671593copy number variation1nstd229human GRCh38 chr2: 6,874,940-6,881,263 , GRCh37.p13 chr2: 7,015,071-7,021,394 RSAD2
    nsv6668408copy number variation1nstd229human GRCh38 chr2: 6,632,294-6,961,758 , GRCh37.p13 chr2: 6,772,426-7,101,889 MIR7515, CMPK2, 8 more genes
    nsv6666576copy number variation1nstd229human GRCh38 chr2: 6,592,339-11,769,396 , GRCh37.p13 chr2: 6,732,471-11,909,522 RN7SKP112, LOC101929861, 103 more genes
    nsv6661381copy number variation1nstd229human GRCh38 chr2: 6,459,726-6,974,378 , GRCh37.p13 chr2: 6,599,858-7,114,509 LOC107985845, LINC01246, 11 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
    nsv6636502copy number variation1nstd102humanUncertain significance GRCh37 chr2: 6,765,428-7,101,997 , GRCh38.p12 chr2: 6,625,296-6,961,866 LOC105373404, MIR7515HG, 8 more genes
    nsv6547376inversion1nstd223human GRCh38 chr2: 6,890,376-6,891,661 , GRCh37.p13 chr2: 7,030,507-7,031,792 RSAD2
    nsv6352412copy number variation1nstd223human GRCh38 chr2: 6,898,602-6,902,905 , GRCh37.p13 chr2: 7,038,733-7,043,036 RSAD2
    nsv6349392copy number variation1nstd223human GRCh38 chr2: 6,874,940-6,881,263 , GRCh37.p13 chr2: 7,015,071-7,021,394 RSAD2
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314874copy number variation1nstd102humanUncertain significance GRCh38 chr2: 6,154,935-7,419,585 , GRCh37.p13 chr2: 6,295,067-7,559,716 LOC107985845, LOC105373402, 20 more genes
    nsv6296158copy number variation1nstd186human GRCh37 chr2: 7,007,539-7,008,077 , GRCh38.p12 chr2: 6,867,408-6,867,946 RSAD2
    nsv6290392copy number variation1nstd102humanUncertain significance GRCh37 chr2: 6,297,801-7,555,446 , GRCh38.p12 chr2: 6,157,669-7,415,315 LOC105373404, LOC105373401, 19 more genes
    nsv6134361copy number variation1nstd213human GRCh37 chr2: 7,000,000-7,130,001 , GRCh38.p12 chr2: 6,859,869-6,989,870 RNF144A, RSAD2, 2 more genes
    nsv5684685mobile element insertion1nstd211human GRCh38 chr2: 6,874,290-6,874,290 , GRCh37.p13 chr2: 7,014,421-7,014,421 RSAD2
    nsv5434872copy number variation1nstd206human GRCh38 chr2: 6,867,408-6,867,946 , GRCh37.p13 chr2: 7,007,539-7,008,077 RSAD2
    nsv5409441mobile element insertion1nstd206human GRCh38 chr2: 6,874,290-6,874,341 , GRCh37.p13 chr2: 7,014,421-7,014,472 RSAD2
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