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Items: 1 to 20 of 571

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146132insertion1nstd232human GRCh37.p13 chr16: 89,684,115-89,684,115 , GRCh38.p12 chr16: 89,617,707-89,617,707 DPEP1
    nsv7141740insertion1nstd232human GRCh37.p13 chr16: 89,701,588-89,701,588 , GRCh38.p12 chr16: 89,635,180-89,635,180 DPEP1
    nsv7139565copy number variation1nstd232human GRCh37.p13 chr16: 89,680,311-89,680,365 , GRCh38.p12 chr16: 89,613,903-89,613,957 DPEP1
    nsv7095062copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,556,653-89,851,392 , GRCh38.p12 chr16: 89,490,245-89,784,984 SNORD68, CHMP1A, 15 more genes
    nsv7095060copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,167,090-89,883,023 , GRCh38.p12 chr16: 89,100,682-89,816,615 VPS9D1, ZNF276, 26 more genes
    nsv7094940copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,611,036-90,106,937 , GRCh38.p12 chr16: 89,544,628-90,040,529 SPATA2L, LINC02166, 25 more genes
    nsv7094939copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,371,594-89,730,828 , GRCh38.p12 chr16: 89,305,186-89,664,420 LOC101930112, LOC101927863, 12 more genes
    nsv7094704copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,334,886-89,723,996 , GRCh38.p12 chr16: 89,268,478-89,657,588 LOC101930112, LOC101927863, 13 more genes
    nsv7094699copy number variation2nstd102humanUncertain significance GRCh37 chr16: 87,636,753-90,109,753 , GRCh38.p12 chr16: 87,603,147-90,043,345 HSALR1, LOC105371412, 87 more genes
    nsv7073763inversion1nstd229human GRCh38 chr16: 89,536,886-89,757,402 , GRCh37.p13 chr16: 89,603,294-89,823,810 SPATA33, SNORD68, 12 more genes
    nsv6998008copy number variation1nstd229human GRCh38 chr16: 89,626,406-89,631,778 , GRCh37.p13 chr16: 89,692,814-89,698,186 DPEP1
    nsv6997823copy number variation1nstd229human GRCh38 chr16: 89,630,157-89,815,080 , GRCh37.p13 chr16: 89,696,565-89,881,488 VPS9D1-AS1, CDK10, 8 more genes
    nsv6995724copy number variation1nstd229human GRCh38 chr16: 89,606,462-89,615,812 , GRCh37.p13 chr16: 89,672,870-89,682,220 DPEP1
    nsv6995211copy number variation1nstd229human GRCh38 chr16: 89,417,001-89,678,600 , GRCh37.p13 chr16: 89,483,409-89,745,008 LOC101927817, CPNE7, 11 more genes
    nsv6994564copy number variation1nstd229human GRCh38 chr16: 89,640,265-89,640,654 , GRCh37.p13 chr16: 89,706,673-89,707,062 DPEP1
    nsv6992944copy number variation1nstd229human GRCh38 chr16: 89,301,591-89,661,186 , GRCh37.p13 chr16: 89,367,999-89,727,594 CMPK1P2, LOC101927863, 12 more genes
    nsv6985866copy number variation1nstd229human GRCh38 chr16: 89,473,541-89,719,269 , GRCh37.p13 chr16: 89,539,949-89,785,677 ANKRD11, SPATA33, 14 more genes
    nsv6984046copy number variation1nstd229human GRCh38 chr16: 89,638,237-89,638,265 , GRCh37.p13 chr16: 89,704,645-89,704,673 DPEP1
    nsv6982338copy number variation1nstd229human GRCh38 chr16: 89,606,222-89,817,329 , GRCh37.p13 chr16: 89,672,630-89,883,737 SPATA33, CHMP1A, 8 more genes
    nsv6981920copy number variation1nstd229human GRCh38 chr16: 89,589,701-89,705,900 , GRCh37.p13 chr16: 89,656,109-89,772,308 SPATA33, CHMP1A, 6 more genes
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