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Items: 1 to 20 of 272

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5674219copy number variation1nstd102humanPathogenic GRCh37 chrX: 84,534,427-85,302,634 , GRCh38.p12 chrX: 85,279,421-86,047,630 MIR1321, CHM, 3 more genes
    nsv5381721copy number variation1nstd102humanUncertain significance GRCh37 chrX: 85,090,756-85,404,112 , GRCh38.p12 chrX: 85,835,751-86,149,108 TPMTP4, CHM, 6 more genes
    nsv5163875mobile element insertion1nstd203human GRCh38 chrX: 85,903,569-85,903,584 , GRCh37.p13 chrX: 85,158,574-85,158,589 CHM, MIR361
    nsv5059979copy number variation1nstd102humanPathogenic GRCh37 chrX: 56,469,080-155,233,731 , GRCh38.p12 chrX: 56,442,647-156,004,066 VDAC1P1, LOC105373299, 1364 more genes
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 more genes
    nsv4769249copy number variation1nstd201human GRCh37 chrX: 61,728,816-155,233,846 , GRCh38.p12 chrX: 62,509,346-156,004,181 , ABCB7, 1364 more genes
    nsv4728601copy number variation1nstd102humanPathogenic GRCh37 chrX: 77,514,079-127,770,854 , GRCh38.p12 chrX: 78,258,582-128,636,876 PHB1P10, SNORA35, 565 more genes
    nsv4728511copy number variation1nstd102humanUncertain significance GRCh37 chrX: 85,002,027-85,171,444 , GRCh38.p12 chrX: 85,747,022-85,916,439 CHM, SFR1P2, 2 more genes
    nsv4728499copy number variation1nstd102humanPathogenic GRCh37 chrX: 55,507,789-155,198,481 , GRCh38.p12 chrX: 55,481,356-155,968,816 GABRE, RN7SL325P, 1371 more genes
    nsv4684016inversion1nstd191human GRCh37.p13 chrX: 32,933,886-87,244,324 , GRCh38 chrX: 32,915,769-87,989,324 , ABCB7, 816 more genes
    nsv4683737copy number variation1nstd102humanPathogenic GRCh37 chrX: 83,372,068-86,890,775 , GRCh38.p12 chrX: 84,117,060-87,635,775 DACH2, GEMIN8P3, 22 more genes
    nsv4683705copy number variation1nstd102humanUncertain significance GRCh37 chrX: 85,090,756-85,166,343 , GRCh38.p12 chrX: 85,835,751-85,911,338 CHM, MIR1321, 2 more genes
    nsv4683459copy number variation1nstd102humanPathogenic GRCh37 chrX: 83,126,460-86,924,394 , GRCh38.p12 chrX: 83,871,452-87,669,394 SFR1P2, SETP4, 23 more genes
    nsv4683359copy number variation1nstd102humanPathogenic GRCh37 chrX: 83,576,897-86,924,394 , GRCh38.p12 chrX: 84,321,889-87,669,394 SATL1, TPMTP4, 20 more genes
    nsv4682957copy number variation1nstd102humanPathogenic GRCh37 chrX: 82,763,333-86,890,775 , GRCh38.p12 chrX: 83,508,325-87,635,775 KLHL4, ZNF711, 26 more genes
    nsv4682948copy number variation1nstd102humanPathogenic GRCh37 chrX: 82,763,333-86,924,394 , GRCh38.p12 chrX: 83,508,325-87,669,394 EEF1A1P29, POMPP1, 26 more genes
    nsv4682751copy number variation1nstd102humanPathogenic GRCh37 chrX: 85,133,970-85,158,746 , GRCh38.p12 chrX: 85,878,965-85,903,741 CHM, MIR361
    nsv4682132copy number variation1nstd102humanPathogenic GRCh37 chrX: 84,634,178-85,404,112 , GRCh38.p12 chrX: 85,379,173-86,149,108 CHM, POF1B, 7 more genes
    nsv4682126copy number variation1nstd102humanPathogenic GRCh37 chrX: 85,090,756-86,924,394 , GRCh38.p12 chrX: 85,835,751-87,669,394 KLHL4, MIR1321, 11 more genes
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