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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
    esv2938506insertion1estd209human GRCh37 chr16: 3,234,623-3,234,623 , GRCh38.p12 chr16: 3,184,623-3,184,623 TRP-TGG3-4
    nsv1826348short tandem repeat4nstd128human GRCh37 chr16: 3,234,624-3,234,649 , GRCh38.p12 chr16: 3,184,624-3,184,649 TRP-TGG3-4
    nsv1826098short tandem repeat3nstd128human GRCh37 chr16: 3,234,218-3,234,241 , GRCh38.p12 chr16: 3,184,218-3,184,241 TRP-TGG3-4
    nsv5514254copy number variation1nstd206human GRCh38 chr16: 3,182,635-3,184,208 , GRCh37.p13 chr16: 3,232,635-3,234,208 TRP-AGG2-7, TRP-TGG3-4
    esv3876447copy number variation2estd219human GRCh37 chr16: 3,232,625-3,234,201 , GRCh38.p12 chr16: 3,182,625-3,184,201 TRP-TGG3-4, TRP-AGG2-7
    esv3637656copy number variation2estd214human GRCh37 chr16: 3,232,625-3,234,201 , GRCh38.p12 chr16: 3,182,625-3,184,201 TRP-TGG3-4, TRP-AGG2-7
    nsv6959918copy number variation1nstd229human GRCh38 chr16: 3,182,393-3,185,213 , GRCh37.p13 chr16: 3,232,393-3,235,213 TRP-AGG2-7, TRP-TGG3-4
    nsv1826345short tandem repeat1nstd128human GRCh37 chr16: 3,232,514-3,232,529 , GRCh38.p12 chr16: 3,182,514-3,182,529 TRP-TGG3-4, TRP-AGG2-7
    nsv6577589inversion1nstd223human GRCh38 chr16: 3,184,189-3,188,147 , GRCh37.p13 chr16: 3,234,189-3,238,147 OR1F1, TRP-TGG3-5, 2 more genes
    nsv3912877copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,900,735-7,160,698 , NCBI36 chr16: 2,840,736-7,100,699 , GRCh38 chr16: 2,850,734-7,110,697 TRP-CGG1-2, RBFOX1, 129 more genes
    nsv3909798copy number variation1nstd102humanPathogenic GRCh37 chr16: 3,146,027-6,362,229 , GRCh38.p12 chr16: 3,096,026-6,312,228 LINC01569, LOC105371062, 102 more genes
    nsv3911457copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,544,805-3,296,579 , GRCh38 chr16: 2,494,804-3,246,579 , NCBI36 chr16: 2,484,806-3,236,580 SNORA3C, PKMYT1, 70 more genes
    nsv3906108copy number variation1nstd102humanPathogenic GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224 CKLF, NPIPP1, 1882 more genes
    nsv3904593copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973 LOC100128079, LOC105379474, 1879 more genes
    nsv3901410copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287 LINC02175, FCSK, 1877 more genes
    nsv3909417copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867 PRSS53, LINC02134, 1868 more genes
    nsv3892266copy number variation2nstd102humanPathogenic GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654 FTLP14, ZNF785, 1868 more genes
    nsv1398297copy number variation1nstd102humanPathogenic GRCh37 chr16: 102,839-28,327,676 , GRCh38.p12 chr16: 52,839-28,316,355 BMERB1, LOC105371094, 701 more genes
    nsv4729901copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,959,279-30,190,593 , GRCh38.p12 chr16: 2,909,278-30,179,272 NPIPB9, TMEM219, 597 more genes
    nsv3903116copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-22,442,007 , GRCh38.p12 chr16: 35,880-22,430,686 NPIPA8, MPG, 616 more genes
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