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Items: 1 to 20 of 331

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7055123inversion1nstd229human GRCh38 chr2: 23,920,765-23,945,500 , GRCh37.p13 chr2: 24,143,635-24,168,370 UBXN2A, SDHCP3, 1 more genes
    nsv7048748inversion1nstd229human GRCh38 chr2: 23,996,296-24,002,192 , GRCh37.p13 chr2: 24,219,166-24,225,062 RN7SL610P, UBXN2A
    nsv7045915inversion1nstd229human GRCh38 chr2: 23,929,190-23,929,358 , GRCh37.p13 chr2: 24,152,060-24,152,228 UBXN2A
    nsv7044920inversion1nstd229human GRCh38 chr2: 23,929,217-23,929,321 , GRCh37.p13 chr2: 24,152,087-24,152,191 UBXN2A
    nsv7044864inversion1nstd229human GRCh38 chr2: 23,929,195-23,929,328 , GRCh37.p13 chr2: 24,152,065-24,152,198 UBXN2A
    nsv6676890copy number variation1nstd229human GRCh38 chr2: 23,963,439-24,043,304 , GRCh37.p13 chr2: 24,186,309-24,266,174 FKBP1B, RN7SL610P, 3 more genes
    nsv6673794copy number variation1nstd229human GRCh38 chr2: 23,958,950-23,976,082 , GRCh37.p13 chr2: 24,181,820-24,198,952 UBXN2A
    nsv6673505copy number variation1nstd229human GRCh38 chr2: 23,987,607-23,993,430 , GRCh37.p13 chr2: 24,210,477-24,216,300 UBXN2A
    nsv6671602copy number variation1nstd229human GRCh38 chr2: 23,977,978-23,984,940 , GRCh37.p13 chr2: 24,200,848-24,207,810 UBXN2A
    nsv6671407copy number variation1nstd229human GRCh38 chr2: 23,910,948-23,925,624 , GRCh37.p13 chr2: 24,133,818-24,148,494 ATAD2B, UBXN2A
    nsv6669650copy number variation1nstd229human GRCh38 chr2: 23,961,245-23,961,758 , GRCh37.p13 chr2: 24,184,115-24,184,628 UBXN2A
    nsv6666873copy number variation1nstd229human GRCh38 chr2: 23,622,207-24,033,282 , GRCh37.p13 chr2: 23,845,077-24,256,152 SDHCP3, KLHL29, 8 more genes
    nsv6663753copy number variation1nstd229human GRCh38 chr2: 23,971,901-23,974,900 , GRCh37.p13 chr2: 24,194,771-24,197,770 UBXN2A
    nsv6663543copy number variation1nstd229human GRCh38 chr2: 23,871,801-24,132,500 , GRCh37.p13 chr2: 24,094,671-24,355,370 SF3B6, WDCP, 12 more genes
    nsv6660386copy number variation1nstd229human GRCh38 chr2: 23,946,694-24,004,795 , GRCh37.p13 chr2: 24,169,564-24,227,665 RN7SL610P, UBXN2A
    nsv6660346copy number variation1nstd229human GRCh38 chr2: 23,927,216-23,927,254 , GRCh37.p13 chr2: 24,150,086-24,150,124 ATAD2B, UBXN2A
    nsv6658790copy number variation1nstd229human GRCh38 chr2: 23,928,345-23,931,783 , GRCh37.p13 chr2: 24,151,215-24,154,653 UBXN2A
    nsv6637009copy number variation1nstd102humanUncertain significance GRCh37 chr2: 23,908,436-24,636,185 , GRCh38.p12 chr2: 23,685,566-24,413,316 HMGN2P20, KLHL29, 19 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
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