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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3165123copy number variation3nstd151human GRCh37 (hg19) chr17: 75,212,628-75,212,651 , GRCh38 (hg38) chr17: 77,216,546-77,216,569 SEC14L1
    nsv3162617copy number variation1nstd151human GRCh37 (hg19) chr17: 75,209,997-75,303,282 , GRCh38 (hg38) chr17: 77,213,915-77,307,200 , GRCh38.p2 chr17|NW_003315955.1: 1,976-90,219 SEC14L1, LOC105371907, 3 more genes
    nsv3162362copy number variation2nstd151human GRCh37 (hg19) chr17: 75,208,029-75,212,651 , GRCh38 (hg38) chr17: 77,211,947-77,216,569 SEC14L1
    nsv3161072copy number variation1nstd151human GRCh37 (hg19) chr17: 75,212,628-75,303,282 , GRCh38 (hg38) chr17: 77,216,546-77,307,200 , GRCh38.p2 chr17|NW_003315955.1: 1,976-90,219 SEC14L1, SEPT9, 3 more genes
    nsv3159405copy number variation1nstd151human GRCh37 (hg19) chr17: 75,085,388-75,085,578 , GRCh38 (hg38) chr17: 77,089,306-77,089,496 SEC14L1, SCARNA16, 2 more genes
    esv4010450copy number variation1estd233human GRCh37 (hg19) chr17: 74,666,000-77,991,000 , GRCh38 (hg38) chr17: 76,669,918-80,017,201 SEC14L1, BIRC5, 89 more genes
    nsv3056233insertion1nstd140human GRCh38 (hg38) chr17: 77,103,707-77,103,708 , GRCh37 (hg19) chr17: 75,099,789-75,099,790 SEC14L1
    nsv2798065insertion1nstd137human GRCh38 (hg38) chr17: 77,103,707-77,103,707 , GRCh37 (hg19) chr17: 75,099,789-75,099,789 SEC14L1
    nsv2779082copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr17: 42,580,684-81,085,615 , GRCh38 (hg38) chr17: 44,503,316-83,137,846 , NCBI36 (hg18) chr17: 39,936,210-78,641,478 SEC14L1, ACTG1, 998 more genes
    nsv2779064copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr17: 67,002,415-81,041,938 , GRCh38 (hg38) chr17: 69,006,274-83,084,062 , NCBI36 (hg18) chr17: 64,514,010-78,635,227 SEC14L1, LOC105274304, 397 more genes
    nsv2778854copy number variation2nstd37humanPathogenic GRCh37 (hg19) chr17: 73,951,701-81,041,938 , GRCh38 (hg38) chr17: 75,955,620-83,084,062 , NCBI36 (hg18) chr17: 71,463,296-78,635,227 SEC14L1, LGALS3BP, 247 more genes
    nsv2777361copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr17: 31,824,931-78,654,742 , GRCh37 (hg19) chr17: 34,750,818-81,048,189 , GRCh38 (hg38) chr17: 36,321,896-83,103,577 SEC14L1, AANAT, 1395 more genes
    nsv2776429copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr17: 73,992,637-75,099,218 , GRCh38 (hg38) chr17: 75,996,556-77,103,136 , NCBI36 (hg18) chr17: 71,504,232-72,610,813 SEC14L1, EVPL, 53 more genes
    nsv2774357copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr17: 16,698,288-78,654,742 , GRCh37 (hg19) chr17: 16,757,563-81,048,189 , GRCh38 (hg38) chr17: 16,854,249-83,103,577 SEC14L1, ASIC2, 1919 more genes
    nsv2773934copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr17: 75,104,943-75,602,123 , GRCh38 (hg38) chr17: 77,108,861-77,606,041 , NCBI36 (hg18) chr17: 72,616,538-73,113,718 SEC14L1, MIR4316, 12 more genes
    nsv2770241copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr17: 64,241,326-81,041,938 , GRCh38 (hg38) chr17: 66,245,208-83,084,062 , NCBI36 (hg18) chr17: 61,671,788-78,635,227 SEC14L1, ACOX1, 447 more genes
    nsv2769779copy number variation2nstd37humanPathogenic GRCh37 (hg19) chr17: 526-81,041,938 , GRCh38 (hg38) chr17: 150,733-83,084,062 , NCBI36 (hg18) chr17: 526-78,635,227 SEC14L1, VMO1, 2440 more genes
    esv3880422copy number variation1estd219human GRCh37 (hg19) chr17: 75,061,606-75,177,066 , GRCh38 (hg38) chr17: 77,065,524-77,180,984 SEC14L1, MIR6516, 5 more genes
    nsv2750244copy number variation2nstd130human NCBI36 (hg18) chr17: 72,567,515-72,609,505 , GRCh37 (hg19) chr17: 75,055,920-75,097,910 , GRCh38 (hg38) chr17: 77,059,838-77,101,828 SEC14L1, SCARNA16, 2 more genes
    nsv1899754short tandem repeat8nstd128human GRCh37 (hg19) chr17: 75,199,002-75,199,034 , GRCh38 (hg38) chr17: 77,202,920-77,202,952 SEC14L1
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