U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 340

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3906859copy number variation1nstd102humanBenign GRCh37 chr16: 15,977,824-16,012,829 , GRCh38.p12 chr16: 15,883,967-15,918,972 , GRCh38.p12 chr16|NT_187607.1: 1,541,968-1,576,935 CEP20, LOC107984869
    nsv3900280copy number variation1nstd102humanBenign GRCh37 chr16: 15,977,824-16,012,820 , GRCh38.p12 chr16: 15,883,967-15,918,963 , GRCh38.p12 chr16|NT_187607.1: 1,541,968-1,576,926 CEP20, LOC107984869
    nsv3894537copy number variation1nstd102humanBenign GRCh37 chr16: 15,973,076-16,005,568 , GRCh38.p12 chr16: 15,879,219-15,911,711 , GRCh38.p12 chr16|NT_187607.1: 1,537,214-1,569,699 CEP20, LOC107984869
    nsv3905230copy number variation1nstd102humanBenign GRCh37 chr16: 15,980,247-16,040,539 , GRCh38.p12 chr16|NT_187607.1: 1,544,391-1,604,656 , GRCh38.p12 chr16: 15,886,390-15,946,682 CEP20, RPL15P20, 1 more genes
    nsv3905801copy number variation1nstd102humanBenign GRCh37 chr16: 15,959,456-16,014,540 , GRCh38.p12 chr16: 15,865,599-15,920,683 , GRCh38.p12 chr16|NT_187607.1: 1,523,598-1,578,646 CEP20, LOC107984869, 1 more genes
    nsv3896414copy number variation1nstd102humanUncertain significance GRCh37 chr16: 15,939,427-15,979,664 , GRCh38.p12 chr16|NT_187607.1: 1,503,560-1,543,808 , GRCh38.p12 chr16: 15,845,570-15,885,807 CEP20, RNU6-213P, 1 more genes
    nsv3885195copy number variation1nstd102humanPathogenic GRCh38 chr16: 15,788,690-16,185,034 , GRCh37.p13 chr16: 15,882,547-16,278,891 CEP20, ABCC6, 6 more genes
    nsv3916649copy number variation1nstd102humanPathogenic NCBI36 chr16: 14,760,627-18,687,298 , GRCh37.p13 chr16: 14,853,126-18,779,797 , GRCh38.p12 chr16: 14,759,269-18,768,475 , GRCh38.p12 chr16|NT_187607.1: 293,011-2,659,700 CEP20, RRN3, 90 more genes
    nsv3920316copy number variation1nstd102humanPathogenic GRCh38 chr16: 14,816,348-18,658,403 , NCBI36 chr16: 14,817,706-18,577,226 , GRCh37 chr16: 14,910,205-18,669,725 CEP20, MIR6511A1, 82 more genes
    nsv3904576copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,318,664-18,778,064 , GRCh38.p12 chr16: 15,224,807-18,766,742 CEP20, RPL7P47, 58 more genes
    nsv3923793copy number variation1nstd102humanPathogenic NCBI36 chr16: 15,141,934-18,577,226 , GRCh37 chr16: 15,234,433-18,669,725 , GRCh38 chr16: 15,140,576-18,658,403 CEP20, LOC102723692, 62 more genes
    nsv3921429copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,917,806-18,149,685 , GRCh38 chr16: 14,823,949-18,055,828 , NCBI36 chr16: 14,825,307-18,057,186 CEP20, NOMO1, 61 more genes
    nsv3922278copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,910,205-18,141,051 , GRCh38 chr16: 14,816,348-18,047,194 , NCBI36 chr16: 14,817,706-18,048,552 CEP20, MIR6770-1, 61 more genes
    nsv3904490copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,316,618-18,181,971 , GRCh38.p12 chr16: 15,222,761-18,088,114 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-2,659,700 CEP20, NDE1, 37 more genes
    nsv7148112copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,489,453-18,321,582 , GRCh38.p12 chr16: 15,395,596-18,227,725 , GRCh38.p12 chr16|NT_187607.1: 1,053,559-2,659,700 CEP20, MIR484, 37 more genes
    nsv4729445copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,375,911-18,198,455 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-2,659,700 , GRCh38.p12 chr16: 15,282,054-18,104,598 CEP20, BMERB1, 38 more genes
    nsv4674979copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,416,364-18,231,275 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-2,659,700 , GRCh38.p12 chr16: 15,322,507-18,137,418 CEP20, TCERG1P2, 37 more genes
    nsv3914781copy number variation1nstd102humanPathogenic NCBI36 chr16: 15,458,563-18,214,342 , GRCh37 chr16: 15,551,062-18,306,841 , GRCh38 chr16: 15,457,205-18,212,984 CEP20, RPL7P47, 36 more genes
    nsv3895083copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,481,920-18,181,971 , GRCh38.p12 chr16|NT_187607.1: 1,046,027-2,659,700 , GRCh38.p12 chr16: 15,388,063-18,088,114 CEP20, MIR6770-2, 35 more genes
    nsv3924171copy number variation1nstd102humanPathogenic NCBI36 chr16: 15,399,808-18,069,668 , GRCh38 chr16: 15,398,450-18,068,310 , GRCh37 chr16: 15,492,307-18,162,167 CEP20, LOC105371100, 35 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center