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Items: 1 to 20 of 171

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095021copy number variation1nstd102humanUncertain significance GRCh37 chr16: 46,694,384-46,746,708 , GRCh38.p12 chr16: 46,660,472-46,712,796 ORC6, VPS35, 1 more genes
    nsv7094672copy number variation1nstd102humanUncertain significance GRCh37 chr16: 46,694,384-48,258,199 , GRCh38.p12 chr16: 46,660,472-48,224,288 LOC100420642, ITFG1-AS1, 26 more genes
    nsv7061087inversion1nstd229human GRCh38 chr16: 46,572,464-46,738,452 , GRCh37.p13 chr16: 46,606,376-46,772,364 SHCBP1, RAB43P1, 5 more genes
    nsv6994542copy number variation1nstd229human GRCh38 chr16: 46,698,074-46,698,170 , GRCh37.p13 chr16: 46,731,986-46,732,082 ORC6
    nsv6984463copy number variation1nstd229human GRCh38 chr16: 46,673,251-46,798,889 , GRCh37.p13 chr16: 46,707,163-46,832,801 C16orf87, VPS35, 3 more genes
    nsv6978529copy number variation1nstd229human GRCh38 chr16: 46,631,001-46,851,400 , GRCh37.p13 chr16: 46,664,913-46,885,312 LOC100130180, VPS35, 4 more genes
    nsv6978445copy number variation1nstd229human GRCh38 chr16: 46,572,501-46,734,400 , GRCh37.p13 chr16: 46,606,413-46,768,312 ORC6, SHCBP1, 5 more genes
    nsv6637591copy number variation1nstd102humanUncertain significance GRCh37 chr16: 46,503,407-46,860,107 , GRCh38.p12 chr16: 46,469,495-46,826,195 MYLK3, LOC441768, 9 more genes
    nsv6637586copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,573-62,203,182 , GRCh38.p12 chr16: 46,469,661-62,169,278 LINC02140, LOC100130602, 279 more genes
    nsv6623474copy number variation1nstd224human GRCh37 chr16: 46,539,392-46,784,220 , GRCh38.p12 chr16: 46,505,480-46,750,308 ORC6, VPS35, 7 more genes
    nsv6501858copy number variation1nstd223human GRCh38 chr16: 46,673,251-46,798,889 , GRCh37.p13 chr16: 46,707,163-46,832,801 LOC100130180, VPS35, 3 more genes
    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
    nsv6309909copy number variation3nstd102humanUncertain significance GRCh37 chr16: 46,694,384-46,782,105 , GRCh38.p12 chr16: 46,660,472-46,748,193 VPS35, MYLK3, 1 more genes
    nsv6309868copy number variation1nstd102humanUncertain significance GRCh37 chr16: 46,694,384-46,755,125 , GRCh38.p12 chr16: 46,660,472-46,721,213 ORC6, VPS35, 1 more genes
    nsv6291594copy number variation1nstd102humanUncertain significance GRCh37 chr16: 46,503,328-47,004,071 , GRCh38.p12 chr16: 46,469,416-46,970,159 ANKRD26P1, RNU6-845P, 13 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
    nsv6132991copy number variation1nstd213human GRCh37 chr16: 46,460,000-48,129,895 , GRCh38.p12 chr16: 46,426,088-48,095,984 CKBP1, PHKB, 31 more genes
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv6024630copy number variation1nstd212human GRCh38 chr16: 46,694,421-46,694,601 , GRCh37.p13 chr16: 46,728,333-46,728,513 ORC6
    nsv5708954mobile element insertion2nstd211human GRCh38 chr16: 46,691,595-46,691,595 , GRCh37.p13 chr16: 46,725,507-46,725,507 ORC6
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