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Items: 1 to 20 of 244

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143879copy number variation1nstd232human GRCh37.p13 chr16: 75,488,049-75,488,135 , GRCh38.p12 chr16: 75,454,151-75,454,237 TMEM170A
    nsv7065292inversion1nstd229human GRCh38 chr16: 75,462,020-75,509,475 , GRCh37.p13 chr16: 75,495,918-75,543,373 CHST6, TMEM231P1, 1 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
    nsv6998053copy number variation1nstd229human GRCh38 chr16: 75,164,533-76,191,896 , GRCh37.p13 chr16: 75,198,431-76,225,794 CTRB2, LOC105371344, 25 more genes
    nsv6994660copy number variation1nstd229human GRCh38 chr16: 75,461,213-75,461,259 , GRCh37.p13 chr16: 75,495,111-75,495,157 TMEM170A
    nsv6993370copy number variation1nstd229human GRCh38 chr16: 75,442,466-75,610,207 , GRCh37.p13 chr16: 75,476,364-75,644,105 ADAT1, TMEM231, 5 more genes
    nsv6992741copy number variation1nstd229human GRCh38 chr16: 75,460,918-75,508,723 , GRCh37.p13 chr16: 75,494,816-75,542,621 CHST6, TMEM231P1, 1 more genes
    nsv6991990copy number variation1nstd229human GRCh38 chr16: 75,454,151-75,454,238 , GRCh37.p13 chr16: 75,488,049-75,488,136 TMEM170A
    nsv6989289copy number variation1nstd229human GRCh38 chr16: 75,389,676-75,513,378 , GRCh37.p13 chr16: 75,423,574-75,547,276 CFDP1, TMEM231P1, 2 more genes
    nsv6988482copy number variation1nstd229human GRCh38 chr16: 75,449,701-75,453,400 , GRCh37.p13 chr16: 75,483,599-75,487,298 TMEM170A
    nsv6987788copy number variation1nstd229human GRCh38 chr16: 75,437,833-75,452,323 , GRCh37.p13 chr16: 75,471,731-75,486,221 TMEM170A
    nsv6982168copy number variation1nstd229human GRCh38 chr16: 75,455,769-75,473,258 , GRCh37.p13 chr16: 75,489,667-75,507,156 CHST6, TMEM170A
    nsv6978828copy number variation1nstd229human GRCh38 chr16: 75,289,102-75,918,471 , GRCh37.p13 chr16: 75,323,000-75,952,369 KARS1, LOC105371348, 16 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
    nsv6593843inversion1nstd223human GRCh38 chr16: 75,458,932-75,459,742 , GRCh37.p13 chr16: 75,492,830-75,493,640 TMEM170A
    nsv6583345inversion1nstd223human GRCh38 chr16: 75,448,675-75,449,422 , GRCh37.p13 chr16: 75,482,573-75,483,320 TMEM170A
    nsv6510366copy number variation1nstd223human GRCh38 chr16: 75,454,151-75,454,238 , GRCh37.p13 chr16: 75,488,049-75,488,136 TMEM170A
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