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Items: 1 to 20 of 23

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3891544copy number variation1nstd102humanBenign GRCh37 chr14: 66,034,586-66,055,943 , GRCh38.p12 chr14: 65,567,868-65,589,225 FUT8
    nsv3899215copy number variation1nstd102humanBenign GRCh37 chr14: 66,034,586-66,052,460 , GRCh38.p12 chr14: 65,567,868-65,585,742 FUT8
    nsv3907451copy number variation1nstd102humanBenign GRCh37 chr14: 66,046,816-66,052,713 , GRCh38.p12 chr14: 65,580,098-65,585,995 FUT8
    nsv4728797copy number variation1nstd102humanLikely benign GRCh37 chr14: 65,998,774-66,403,585 , GRCh38.p12 chr14: 65,532,056-65,936,867 FUT8, FTH1P13, 2 more genes
    nsv6291593copy number variation1nstd102humanUncertain significance GRCh37 chr14: 65,812,267-66,203,014 , GRCh38.p12 chr14: 65,345,549-65,736,296 FUT8, EIF1AXP2, 3 more genes
    nsv4455264copy number variation1nstd102humanUncertain significance GRCh37 chr14: 65,996,716-66,409,522 , GRCh38.p12 chr14: 65,529,998-65,942,804 FUT8, EIF1AXP2, 3 more genes
    nsv4455711copy number variation1nstd102humanUncertain significance GRCh37 chr14: 66,005,150-66,403,417 , GRCh38.p12 chr14: 65,538,432-65,936,699 FUT8, NCOA4P1, 2 more genes
    nsv3922652copy number variation1nstd102humanPathogenic GRCh37 chr14: 57,507,754-67,674,948 , NCBI36 chr14: 56,577,507-66,744,701 , GRCh38 chr14: 57,041,036-67,208,231 FUT8, PARP1P2, 160 more genes
    nsv3923965copy number variation1nstd102humanPathogenic GRCh37 chr14: 60,383,769-67,217,521 , NCBI36 chr14: 59,453,522-66,287,274 , GRCh38 chr14: 59,917,051-66,750,803 FUT8, ESR2, 111 more genes
    nsv3912530copy number variation1nstd102humanPathogenic NCBI36 chr14: 61,789,171-65,289,887 , GRCh38 chr14: 62,252,700-65,753,416 , GRCh37 chr14: 62,719,418-66,220,134 FUT8, MIR625, 59 more genes
    nsv3902883copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,000,422-107,289,053 , GRCh38.p12 chr14: 18,223,945-106,880,863 FUT8, LOC440181, 1998 more genes
    nsv3907460copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456 FUT8, BANF1P1, 1996 more genes
    nsv3899639copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,327,823-107,287,663 , GRCh38.p12 chr14: 18,551,346-106,879,456 FUT8, LOC100289511, 1996 more genes
    nsv3903256copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,794,561-107,234,280 , GRCh38.p12 chr14: 19,652,445-106,826,050 FUT8, DHRS7, 1946 more genes
    nsv3919106copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482 FUT8, SRMP2, 1929 more genes
    nsv3904265copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38.p12 chr14: 20,043,514-106,877,229 FUT8, CRIP1, 1929 more genes
    nsv3917422copy number variation1nstd102humanPathogenic GRCh38 chr14: 20,151,149-106,855,263 , NCBI36 chr14: 19,689,148-106,334,523 , GRCh37 chr14: 20,619,308-107,263,478 FUT8, MIR656, 1918 more genes
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 FUT8, PAPOLA-DT, 1338 more genes
    nsv5980451copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 54,654,001-75,828,024 , GRCh38.p12 chr14: 54,187,283-75,361,321 FUT8, ACTN1, 400 more genes
    nsv3924798copy number variation1nstd102humanUncertain significance NCBI36 chr14: 64,811,144-65,153,598 , GRCh37 chr14: 65,741,391-66,083,845 , GRCh38 chr14: 65,274,673-65,617,127 FUT8, MIR4708, 5 more genes
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