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Items: 1 to 20 of 146

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095097copy number variation1nstd102humanUncertain significance GRCh37 chr16: 75,589,682-75,690,509 , GRCh38.p12 chr16: 75,555,784-75,656,611 GABARAPL2, TMEM231, 3 more genes
    nsv7072367inversion1nstd229human GRCh38 chr16: 75,592,487-75,707,026 , GRCh37.p13 chr16: 75,626,385-75,740,924 TERF2IP, ATP5PBP7, 5 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
    nsv6997748copy number variation1nstd229human GRCh38 chr16: 75,530,336-75,837,326 , GRCh37.p13 chr16: 75,564,234-75,871,224 CPHXL, CPHXL2, 11 more genes
    nsv6993109copy number variation1nstd229human GRCh38 chr16: 75,592,401-75,687,000 , GRCh37.p13 chr16: 75,626,299-75,720,898 ADAT1, TERF2IP, 2 more genes
    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
    nsv6503264copy number variation1nstd223human GRCh38 chr16: 75,643,932-75,645,769 , GRCh37.p13 chr16: 75,677,830-75,679,667 TERF2IP, KARS1
    nsv6314906copy number variation1nstd102humanPathogenic GRCh37 chr16: 75,428,968-75,690,509 , GRCh38.p12 chr16: 75,395,070-75,656,611 GABARAPL2, CHST6, 8 more genes
    nsv6314867copy number variation1nstd102humanUncertain significance GRCh37 chr16: 75,661,793-75,690,509 , GRCh38.p12 chr16: 75,627,895-75,656,611 KARS1, TERF2IP
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6310095copy number variation1nstd102humanPathogenic GRCh37 chr16: 75,573,892-75,690,509 , GRCh38.p12 chr16: 75,539,994-75,656,611 TERF2IP, KARS1, 3 more genes
    nsv6133280copy number variation1nstd213human GRCh37 chr16: 75,630,000-75,690,001 , GRCh38.p12 chr16: 75,596,102-75,656,103 KARS1, ADAT1, 1 more genes
    nsv6133206copy number variation1nstd213human GRCh37 chr16: 74,460,000-84,740,001 , GRCh38.p12 chr16: 74,426,102-84,706,395 , CDH13, 142 more genes
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    nsv5946568copy number variation1nstd209human GRCh38 chr16: 75,651,286-75,651,954 , GRCh37.p13 chr16: 75,685,184-75,685,852 TERF2IP
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