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Items: 1 to 20 of 116

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5967951inversion1nstd209human GRCh38 chr16: 13,469,401-22,726,308 , GRCh37.p13 chr16: 13,563,258-22,737,629 , ABCC6, 214 more genes
    nsv5929387copy number variation1nstd209human GRCh38 chr16: 20,698,055-24,692,430 , GRCh37.p13 chr16: 20,709,377-24,703,751 , ACSM1, 87 more genes
    nsv5528985copy number variation1nstd206human GRCh38 chr16: 20,703,170-20,714,693 , GRCh37.p13 chr16: 20,714,492-20,726,015 LOC100887080
    nsv5527184copy number variation1nstd206human GRCh38 chr16: 20,711,791-20,713,817 , GRCh37.p13 chr16: 20,723,113-20,725,139 LOC100887080
    nsv5003108copy number variation1nstd200human GRCh38 chr16: 20,725,988-20,732,433 , GRCh37.p13 chr16: 20,737,310-20,743,755 THUMPD1, LOC100887080
    nsv4994531copy number variation1nstd200human GRCh38 chr16: 20,541,727-20,721,806 , GRCh37.p13 chr16: 20,553,049-20,733,128 , ACSM2B, 6 more genes
    nsv4850678copy number variation1nstd200human GRCh37 chr16: 20,737,310-20,743,755 , GRCh38.p12 chr16: 20,725,988-20,732,433 THUMPD1, LOC100887080
    nsv4748253copy number variation1nstd199human GRCh37 chr16: 20,729,179-20,729,243 , GRCh38.p12 chr16: 20,717,857-20,717,921 LOC100887080
    nsv4729901copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,959,279-30,190,593 , GRCh38.p12 chr16: 2,909,278-30,179,272 NPIPB9, TMEM219, 597 more genes
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 LOC105371069, PKD1P6-NPIPP1, 654 more genes
    nsv4674963copy number variation1nstd102humanLikely benign GRCh37 chr16: 20,488,078-20,759,727 , GRCh38.p12 chr16: 20,476,756-20,748,405 ACSM1, LOC100887080, 8 more genes
    nsv4629783copy number variation1nstd183human GRCh37 chr16: 20,701,162-21,372,600 , GRCh38.p12 chr16: 20,689,840-21,361,279 REXO5, ZP2, 18 more genes
    nsv4626889copy number variation1nstd183human GRCh37 chr16: 20,711,506-20,760,015 , GRCh38.p12 chr16: 20,700,184-20,748,693 THUMPD1, ACSM3, 1 more genes
    nsv4436312complex substitution1nstd102humanPathogenic GRCh38.p12 chr16: 1,230,041-33,908,091 , GRCh37 chr16: 1,280,042-33,710,558 ABAT, ABCA3, 876 more genes
    nsv4425512copy number variation1nstd174human GRCh37 chr16: 20,533,043-20,742,511 , GRCh38.p12 chr16: 20,521,721-20,731,189 , THUMPD1, 7 more genes
    nsv4322553inversion1nstd166human GRCh37.p13 chr16: 16,634,964-31,736,102 , GRCh38.p12 chr16: 16,541,107-31,724,781 , ALDOA, 403 more genes
    nsv4236931copy number variation1nstd166human GRCh37.p13 chr16: 20,742,436-20,742,516 , GRCh38.p12 chr16: 20,731,114-20,731,194 LOC100887080, THUMPD1
    nsv3917409copy number variation1nstd102humanPathogenic NCBI36 chr16: 14,956,252-28,225,665 , GRCh37 chr16: 15,048,751-28,318,164 , GRCh38 chr16: 14,954,894-28,306,843 SLC7A5P2, TRL-TAG3-1, 251 more genes
    nsv3912562copy number variation1nstd102humanUncertain significance GRCh37 chr16: 20,419,342-21,255,795 , GRCh38 chr16: 20,408,020-21,244,474 , NCBI36 chr16: 20,326,843-21,163,296 REXO5, THUMPD1, 22 more genes
    nsv3910441copy number variation1nstd102humanPathogenic NCBI36 chr16: 4,634,894-29,089,642 , GRCh37 chr16: 4,694,893-29,182,141 , GRCh38 chr16: 4,644,892-29,170,820 LOC729945, LOC102723728, 450 more genes
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