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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093395copy number variation1nstd102humanPathogenic GRCh37 chr12: 64,609,458-70,352,103 , GRCh38.p12 chr12: 64,215,678-69,958,323 TODL, MIR6074, 116 more genes
    nsv7066132inversion1nstd229human GRCh38 chr12: 65,153,239-72,873,965 , GRCh37.p13 chr12: 65,547,019-73,267,745 IL26, RPL7P42, 119 more genes
    nsv7063686inversion1nstd229human GRCh38 chr12: 68,612,002-69,442,420 , GRCh37.p13 chr12: 69,005,782-69,836,200 RAP1B, YEATS4, 21 more genes
    nsv7060197inversion1nstd229human GRCh38 chr12: 64,990,820-72,253,420 , GRCh37.p13 chr12: 65,384,600-72,647,200 LINC02384, LOC105369809, 122 more genes
    nsv7059459inversion1nstd229human GRCh38 chr12: 68,623,271-69,442,390 , GRCh37.p13 chr12: 69,017,051-69,836,170 LOC100507250, RPS26P45, 21 more genes
    nsv6935270copy number variation1nstd229human GRCh38 chr12: 68,749,353-68,749,486 , GRCh37.p13 chr12: 69,143,133-69,143,266 SLC35E3
    nsv6933075copy number variation1nstd229human GRCh38 chr12: 68,494,505-68,795,230 , GRCh37.p13 chr12: 68,888,285-69,189,010 LOC100507250, SNORA70G, 9 more genes
    nsv6933056copy number variation1nstd229human GRCh38 chr12: 68,749,501-68,792,700 , GRCh37.p13 chr12: 69,143,281-69,186,480 LOC100422438, SLC35E3
    nsv6928067copy number variation1nstd229human GRCh38 chr12: 68,742,199-68,750,602 , GRCh37.p13 chr12: 69,135,979-69,144,382 NUP107, SLC35E3
    nsv6927961copy number variation1nstd229human GRCh38 chr12: 68,771,779-68,774,412 , GRCh37.p13 chr12: 69,165,559-69,168,192 SLC35E3
    nsv6926798copy number variation1nstd229human GRCh38 chr12: 68,756,757-68,757,990 , GRCh37.p13 chr12: 69,150,537-69,151,770 SLC35E3
    nsv6925948copy number variation1nstd229human GRCh38 chr12: 68,736,001-68,887,600 , GRCh37.p13 chr12: 69,129,781-69,281,380 MDM2, CPM, 4 more genes
    nsv6925343copy number variation1nstd229human GRCh38 chr12: 68,761,015-68,770,659 , GRCh37.p13 chr12: 69,154,795-69,164,439 SLC35E3
    nsv6922005copy number variation1nstd229human GRCh38 chr12: 68,754,101-68,758,600 , GRCh37.p13 chr12: 69,147,881-69,152,380 SLC35E3
    nsv6920504copy number variation1nstd229human GRCh38 chr12: 68,718,247-69,086,160 , GRCh37.p13 chr12: 69,112,027-69,479,940 LOC100422438, CPM, 7 more genes
    nsv6920288copy number variation1nstd229human GRCh38 chr12: 68,781,069-68,781,123 , GRCh37.p13 chr12: 69,174,849-69,174,903 SLC35E3
    nsv6595209inversion1nstd223human GRCh38 chr12: 66,057,683-70,685,410 , GRCh37.p13 chr12: 66,451,463-71,079,190 PSMC6P2, SNORA70G, 86 more genes
    nsv6594036inversion1nstd223human GRCh38 chr12: 66,057,593-72,798,778 , GRCh37.p13 chr12: 66,451,373-73,192,558 PSMC6P2, SNORA70G, 103 more genes
    nsv6593453inversion1nstd223human GRCh38 chr12: 66,057,683-71,774,167 , GRCh37.p13 chr12: 66,451,463-72,167,947 LOC105369833, RN7SL804P, 96 more genes
    nsv6593094inversion1nstd223human GRCh38 chr12: 66,057,683-74,924,429 , GRCh37.p13 chr12: 66,451,463-75,318,209 MYRFL, OSBPL9P5, 119 more genes
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