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Items: 1 to 20 of 143

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095041copy number variation1nstd102humanUncertain significance GRCh37 chr16: 74,485,954-75,339,100 , GRCh38.p12 chr16: 74,452,056-75,305,202 CTRB1, CTRB2, 19 more genes
    nsv7094598copy number variation1nstd102humanUncertain significance GRCh37 chr16: 74,505,051-74,695,347 , GRCh38.p12 chr16: 74,471,153-74,661,449 RPS10P23, HSPE1P7, 2 more genes
    nsv7076339inversion1nstd229human GRCh38 chr16: 70,122,272-74,889,687 , GRCh37.p13 chr16: 70,156,175-74,923,585 SNORD111B, HCCAT5, 96 more genes
    nsv7066185inversion1nstd229human GRCh38 chr16: 71,798,581-75,423,466 , GRCh37.p13 chr16: 71,832,484-75,457,364 TMPOP2, RPSAP56, 57 more genes
    nsv7061930inversion1nstd229human GRCh38 chr16: 71,759,694-75,426,750 , GRCh37.p13 chr16: 71,793,597-75,460,648 BCAR1, LOC105371343, 57 more genes
    nsv7058675inversion1nstd229human GRCh38 chr16: 67,667,666-75,720,241 , GRCh37.p13 chr16: 67,701,569-75,754,139 RNU6-898P, DPEP2, 199 more genes
    nsv6995906copy number variation1nstd229human GRCh38 chr16: 74,608,938-74,644,002 , GRCh37.p13 chr16: 74,642,836-74,677,900 HSPE1P7, RFWD3
    nsv6990121copy number variation1nstd229human GRCh38 chr16: 74,579,142-74,773,977 , GRCh37.p13 chr16: 74,613,040-74,807,875 FA2H, MLKL, 4 more genes
    nsv6988942copy number variation1nstd229human GRCh38 chr16: 74,613,175-74,620,574 , GRCh37.p13 chr16: 74,647,073-74,654,472 RFWD3, HSPE1P7
    nsv6987859copy number variation1nstd229human GRCh38 chr16: 74,533,101-74,779,800 , GRCh37.p13 chr16: 74,566,999-74,813,698 RPS10P23, HSPE1P7, 5 more genes
    nsv6985437copy number variation1nstd229human GRCh38 chr16: 74,609,301-74,616,800 , GRCh37.p13 chr16: 74,643,199-74,650,698 HSPE1P7
    nsv6983408copy number variation1nstd229human GRCh38 chr16: 74,048,861-75,393,024 , GRCh37.p13 chr16: 74,082,760-75,426,922 PSMD7, RNU6-237P, 28 more genes
    nsv6637595copy number variation1nstd102humanUncertain significance GRCh37 chr16: 73,673,334-78,137,887 , GRCh38.p12 chr16: 73,639,435-78,103,990 CNTNAP4, WDR59, 73 more genes
    nsv6637493copy number variation1nstd102humanUncertain significance GRCh37 chr16: 73,673,334-76,105,189 , GRCh38.p12 chr16: 73,639,435-76,071,291 LOC105371347, LOC105371344, 51 more genes
    nsv6637273copy number variation1nstd102humanUncertain significance GRCh37 chr16: 73,858,079-75,855,162 , GRCh38.p12 chr16: 73,824,180-75,821,264 LOC105371344, CTRB2, 46 more genes
    nsv6634465copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 71,610,276-90,354,753 , GRCh38.p12 chr16: 71,576,373-90,228,345 AP1G1, AFG3L1P, 349 more genes
    nsv6594074inversion1nstd223human GRCh38 chr16: 74,612,165-74,613,100 , GRCh37.p13 chr16: 74,646,063-74,646,998 HSPE1P7
    nsv6590528inversion1nstd223human GRCh38 chr16: 74,610,064-74,611,202 , GRCh37.p13 chr16: 74,643,962-74,645,100 HSPE1P7
    nsv6512246copy number variation1nstd223human GRCh38 chr16: 74,610,843-74,612,186 , GRCh37.p13 chr16: 74,644,741-74,646,084 HSPE1P7
    nsv6315469copy number variation1nstd102humanPathogenic GRCh37 chr16: 68,971,067-74,823,560 , GRCh38.p12 chr16: 68,937,164-74,789,662 ZNF19, RNU7-71P, 128 more genes
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