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Items: 1 to 20 of 203

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980449copy number variation1nstd102humanrisk factor GRCh37 chr3: 195,693,872-197,376,871 , GRCh38.p12 chr3: 195,967,001-197,650,000 RN7SL434P, RNU6-1279P, 54 more genes
    nsv5956791insertion1nstd209human GRCh38 chr3: 196,630,635-196,630,635 , GRCh37.p13 chr3: 196,357,506-196,357,506 LINC01063
    nsv5613924insertion1nstd207human GRCh38 chr3: 196,630,635-196,630,635 , GRCh37.p13 chr3: 196,357,506-196,357,506 LINC01063
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5381417copy number variation1nstd102humanUncertain significance GRCh37 chr3: 195,754,030-196,438,852 , GRCh38.p12 chr3: 196,027,159-196,711,981 PIGX, TM4SF19-DYNLT2B, 28 more genes
    nsv5200370copy number variation1nstd102humanPathogenic GRCh37 chr3: 195,419,168-197,387,258 , GRCh38.p12 chr3: 195,692,297-197,660,387 NCBP2AS2, DLG1-AS1, 67 more genes
    nsv5200362copy number variation1nstd102humanPathogenic GRCh37 chr3: 195,747,856-197,387,258 , GRCh38.p12 chr3: 196,020,985-197,660,387 MIR4797, SDHAP4, 52 more genes
    nsv4728352copy number variation1nstd102humanPathogenic GRCh37 chr3: 195,068,028-197,851,986 , GRCh38.p12 chr3: 195,347,299-198,125,115 MUC20, RPL35A, 95 more genes
    nsv4726518insertion1nstd186human GRCh37 chr3: 196,357,506-196,357,506 , GRCh38.p12 chr3: 196,630,635-196,630,635 LINC01063
    nsv4684449copy number variation1nstd192human GRCh37 chr3: 195,750,741-197,346,566 , GRCh38.p12 chr3: 196,023,870-197,619,695 , BDH1, 51 more genes
    nsv4680890copy number variation1nstd189human GRCh37.p13 chr3: 195,989,217-196,454,296 , GRCh38.p12 chr3: 196,262,346-196,727,425 PCYT1A, UBXN7, 22 more genes
    nsv4679009copy number variation1nstd189human GRCh37.p13 chr3: 195,989,217-196,467,748 , GRCh38.p12 chr3: 196,262,346-196,740,877 PAK2, PCYT1A, 23 more genes
    nsv4674548copy number variation1nstd102humanUncertain significance GRCh37 chr3: 196,244,688-196,535,851 , GRCh38.p12 chr3: 196,517,817-196,808,980 PIGX, FBXO45, 10 more genes
    nsv4674472copy number variation1nstd102humanUncertain significance GRCh37 chr3: 195,848,341-196,426,606 , GRCh38.p12 chr3: 196,121,470-196,699,735 TM4SF19-DYNLT2B, WDR53, 23 more genes
    nsv4674423copy number variation1nstd102humanPathogenic GRCh37 chr3: 195,652,973-197,346,971 , GRCh38.p12 chr3: 195,926,102-197,620,100 LOC100133326, UBXN7-AS1, 54 more genes
    nsv4540386insertion1nstd166human GRCh37.p13 chr3: 196,357,506-196,357,506 , GRCh38.p12 chr3: 196,630,635-196,630,635 LINC01063
    nsv4520252copy number variation1nstd166human GRCh37.p13 chr3: 196,359,282-196,359,721 , GRCh38.p12 chr3: 196,632,411-196,632,850 LINC01063
    nsv4454872copy number variation1nstd102humanPathogenic GRCh37 chr3: 195,700,698-197,386,180 , GRCh38.p12 chr3: 195,973,827-197,659,309 RNU6-1279P, CEP19, 54 more genes
    nsv4452016copy number variation1nstd102humanPathogenic GRCh37 chr3: 195,701,149-197,348,561 , GRCh38.p12 chr3: 195,974,278-197,621,690 PIGZ, RNU6-42P, 52 more genes
    nsv4436392copy number variation1nstd102humanPathogenic GRCh37 chr3: 188,386,566-197,838,262 , GRCh38.p12 chr3: 188,668,778-198,111,391 PPP1R2, GCNT1P3, 194 more genes
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