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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5972552insertion1nstd209human GRCh38 chr15: 73,743,828-73,743,828 , GRCh37.p13 chr15: 74,036,169-74,036,169 INSYN1
    nsv5941265copy number variation1nstd209human GRCh38 chr15: 73,744,891-73,745,061 , GRCh37.p13 chr15: 74,037,232-74,037,402 INSYN1
    nsv5933606copy number variation1nstd209human GRCh38 chr15: 71,577,714-80,433,232 , GRCh37.p13 chr15: 71,870,053-80,725,573 , STRA6, 229 more genes
    nsv5597862copy number variation1nstd207human GRCh38 chr15: 73,744,891-73,745,061 , GRCh37.p13 chr15: 74,037,232-74,037,402 INSYN1
    nsv5530233copy number variation1nstd206human GRCh38 chr15: 73,724,910-73,733,924 , GRCh37.p13 chr15: 74,017,251-74,026,265 INSYN1
    nsv5520922copy number variation1nstd206human GRCh38 chr15: 73,734,912-73,735,103 , GRCh37.p13 chr15: 74,027,253-74,027,444 INSYN1
    nsv5516216copy number variation1nstd206human GRCh38 chr15: 73,744,894-73,745,062 , GRCh37.p13 chr15: 74,037,235-74,037,403 INSYN1
    nsv5391809copy number variation3nstd186human GRCh37 chr15: 74,037,235-74,037,403 , GRCh38.p12 chr15: 73,744,894-73,745,062 INSYN1
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5156180mobile element insertion1nstd203human GRCh38 chr15: 73,743,828-73,743,858 , GRCh37.p13 chr15: 74,036,169-74,036,199 INSYN1
    nsv5150985mobile element insertion1nstd203human GRCh38 chr15: 73,745,810-73,745,810 , GRCh37.p13 chr15: 74,038,151-74,038,151 INSYN1
    nsv5147474mobile element insertion1nstd203human GRCh38 chr15: 73,743,825-73,743,828 , GRCh37.p13 chr15: 74,036,166-74,036,169 INSYN1
    nsv4992317copy number variation1nstd200human GRCh38 chr15: 73,744,894-73,745,062 , GRCh37.p13 chr15: 74,037,235-74,037,403 INSYN1
    nsv4992316copy number variation1nstd200human GRCh38 chr15: 73,724,899-73,733,971 , GRCh37.p13 chr15: 74,017,240-74,026,312 INSYN1
    nsv4992298copy number variation1nstd200human GRCh38 chr15: 73,152,590-82,101,178 , GRCh37.p13 chr15: 73,444,931-82,393,519 , SNUPN, 215 more genes
    nsv4850076copy number variation1nstd200human GRCh37 chr15: 74,037,235-74,037,403 , GRCh38.p12 chr15: 73,744,894-73,745,062 INSYN1
    nsv4741205copy number variation1nstd199human GRCh37 chr15: 74,037,228-74,037,401 , GRCh38.p12 chr15: 73,744,887-73,745,060 INSYN1
    nsv4728893copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 70,268,937-74,098,081 , GRCh38.p12 chr15: 69,976,598-73,805,740 BBS4, FKBP1AP2, 75 more genes
    nsv4655181copy number variation1nstd186human GRCh37 chr15: 74,037,235-74,037,688 , GRCh38.p12 chr15: 73,744,894-73,745,347 INSYN1
    nsv4629847copy number variation1nstd183human GRCh37 chr15: 74,017,262-74,026,265 , GRCh38.p12 chr15: 73,724,921-73,733,924 INSYN1
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