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Items: 1 to 20 of 569

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148212copy number variation1nstd102humanPathogenic GRCh38 chr16: 3,818,098-3,858,843 , GRCh37.p13 chr16: 3,868,099-3,908,844 CREBBP
    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
    nsv7095020copy number variation1nstd102humanPathogenic GRCh37 chr16: 3,823,732-3,831,327 , GRCh38.p12 chr16: 3,773,731-3,781,326 CREBBP
    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
    nsv7094841copy number variation1nstd102humanPathogenic GRCh37 chr16: 3,781,438-3,788,947 , GRCh38.p12 chr16: 3,731,437-3,738,946 CREBBP
    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
    nsv7094671copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,860,584-3,860,800 , GRCh38.p12 chr16: 3,810,583-3,810,799 CREBBP
    nsv7094670copy number variation1nstd102humanPathogenic GRCh37 chr16: 3,786,017-3,860,800 , GRCh38.p12 chr16: 3,736,016-3,810,799 CREBBP
    nsv7094666copy number variation3nstd102humanUncertain significance GRCh37 chr16: 256,302-4,852,572 , GRCh38.p12 chr16: 206,303-4,802,571 DNAAF8, TMEM204, 282 more genes
    nsv7094583copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 3,829,526-3,830,870 , GRCh38.p12 chr16: 3,779,525-3,780,869 CREBBP
    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
    nsv7060749inversion1nstd229human GRCh38 chr16: 3,729,042-3,729,204 , GRCh37.p13 chr16: 3,779,043-3,779,205 CREBBP
    nsv6977989copy number variation1nstd229human GRCh38 chr16: 3,821,505-3,821,855 , GRCh37.p13 chr16: 3,871,506-3,871,856 CREBBP
    nsv6976122copy number variation1nstd229human GRCh38 chr16: 3,868,273-3,868,500 , GRCh37.p13 chr16: 3,918,274-3,918,501 CREBBP
    nsv6974289copy number variation1nstd229human GRCh38 chr16: 3,718,484-3,723,394 , GRCh37.p13 chr16: 3,768,485-3,773,395 CREBBP
    nsv6973348copy number variation1nstd229human GRCh38 chr16: 3,858,600-3,861,810 , GRCh37.p13 chr16: 3,908,601-3,911,811 CREBBP
    nsv6972996copy number variation1nstd229human GRCh38 chr16: 3,822,849-3,847,870 , GRCh37.p13 chr16: 3,872,850-3,897,871 CREBBP
    nsv6971960copy number variation1nstd229human GRCh38 chr16: 3,798,936-3,805,335 , GRCh37.p13 chr16: 3,848,937-3,855,336 CREBBP
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