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Items: 1 to 20 of 498

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098906copy number variation1nstd102humanUncertain significance GRCh38 chr16: 3,499,966-3,774,794 , GRCh37.p13 chr16: 3,549,966-3,824,795 CLUAP1, LOC105371060, 6 more genes
    nsv7098765copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 3,767,420-3,860,782 , GRCh38.p12 chr16: 3,717,419-3,810,781 CREBBP, TRAP1
    nsv7095019copy number variation1nstd102humanPathogenic GRCh37 chr16: 3,721,703-3,790,570 , GRCh38.p12 chr16: 3,671,702-3,740,569 CREBBP, TRAP1
    nsv7095018copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,565,488-3,801,827 , GRCh38.p12 chr16: 3,515,488-3,751,826 TRAP1, NLRC3, 6 more genes
    nsv7094836copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,293,141-5,971,108 , GRCh38.p12 chr16: 3,243,141-5,921,107 MGRN1, CORO7, 76 more genes
    nsv7094669copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,725,305-3,729,811 , GRCh38.p12 chr16: 3,675,304-3,679,810 TRAP1
    nsv7094666copy number variation3nstd102humanUncertain significance GRCh37 chr16: 256,302-4,852,572 , GRCh38.p12 chr16: 206,303-4,802,571 DNAAF8, TMEM204, 282 more genes
    nsv7094582copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,551,068-3,901,030 , GRCh38.p12 chr16: 3,501,068-3,851,029 NLRC3, LOC105371060, 6 more genes
    nsv7073336inversion1nstd229human GRCh38 chr16: 3,659,989-3,665,150 , GRCh37.p13 chr16: 3,709,990-3,715,151 DNASE1, TRAP1
    nsv7064771inversion1nstd229human GRCh38 chr16: 3,661,767-3,665,136 , GRCh37.p13 chr16: 3,711,768-3,715,137 DNASE1, TRAP1
    nsv6977524copy number variation1nstd229human GRCh38 chr16: 3,658,076-3,658,168 , GRCh37.p13 chr16: 3,708,077-3,708,169 DNASE1, TRAP1
    nsv6976866copy number variation1nstd229human GRCh38 chr16: 3,686,038-3,686,221 , GRCh37.p13 chr16: 3,736,039-3,736,222 TRAP1
    nsv6975691copy number variation1nstd229human GRCh38 chr16: 3,693,763-3,698,678 , GRCh37.p13 chr16: 3,743,764-3,748,679 TRAP1
    nsv6975318copy number variation1nstd229human GRCh38 chr16: 3,675,081-3,682,889 , GRCh37.p13 chr16: 3,725,082-3,732,890 TRAP1
    nsv6974191copy number variation1nstd229human GRCh38 chr16: 3,709,936-3,722,294 , GRCh37.p13 chr16: 3,759,937-3,772,295 TRAP1
    nsv6974017copy number variation1nstd229human GRCh38 chr16: 3,696,956-3,706,184 , GRCh37.p13 chr16: 3,746,957-3,756,185 TRAP1
    nsv6971985copy number variation1nstd229human GRCh38 chr16: 3,702,122-3,704,016 , GRCh37.p13 chr16: 3,752,123-3,754,017 TRAP1
    nsv6971301copy number variation1nstd229human GRCh38 chr16: 3,639,521-3,674,061 , GRCh37.p13 chr16: 3,689,522-3,724,062 DNASE1, TRAP1
    nsv6971071copy number variation1nstd229human GRCh38 chr16: 3,698,501-3,700,700 , GRCh37.p13 chr16: 3,748,502-3,750,701 TRAP1
    nsv6969974copy number variation1nstd229human GRCh38 chr16: 3,653,708-3,669,652 , GRCh37.p13 chr16: 3,703,709-3,719,653 DNASE1, TRAP1
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