U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 128

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5890300copy number variation1nstd209human GRCh38 chr3: 184,287,042-184,304,653 , GRCh37.p13 chr3: 184,004,830-184,022,441 EEF1AKMT4-ECE2, PSMD2, 1 more genes
    nsv5835425copy number variation1nstd209human GRCh38 chr3: 184,286,941-184,300,509 , GRCh37.p13 chr3: 184,004,729-184,018,297 EEF1AKMT4-ECE2, PSMD2, 1 more genes
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5442753copy number variation1nstd206human GRCh38 chr3: 184,290,396-184,321,664 , GRCh37.p13 chr3: 184,008,184-184,039,452 EIF4G1, PSMD2, 2 more genes
    nsv5441425copy number variation1nstd206human GRCh38 chr3: 184,287,002-184,304,711 , GRCh37.p13 chr3: 184,004,790-184,022,499 PSMD2, ECE2, 1 more genes
    nsv4924944copy number variation1nstd200human GRCh38 chr3: 184,290,396-184,321,664 , GRCh37.p13 chr3: 184,008,184-184,039,452 ECE2, PSMD2, 2 more genes
    nsv4924942copy number variation1nstd200human GRCh38 chr3: 184,108,733-184,353,203 , GRCh37.p13 chr3: 183,826,521-184,070,991 SNORD66, CAMK2N2, 17 more genes
    nsv4805052copy number variation1nstd200human GRCh37 chr3: 184,004,787-184,022,630 , GRCh38.p12 chr3: 184,286,999-184,304,842 ECE2, EEF1AKMT4-ECE2, 1 more genes
    nsv4769252copy number variation1nstd102humanPathogenic GRCh37 chr3: 181,171,210-184,706,091 , GRCh38.p12 chr3: 181,453,422-184,988,303 LOC107986054, LOC107986160, 83 more genes
    nsv4728604copy number variation1nstd102humanPathogenic GRCh37 chr3: 182,877,291-186,830,759 , GRCh38.p12 chr3: 183,159,503-187,112,971 LOC105374253, GPS2P2, 111 more genes
    nsv4707413translocation1nstd195human GRCh37 chr3: 184,019,847-184,019,847 , GRCh38.p12 chr3: 184,302,059-184,302,059 , GRCh38.p12 chr1: 240,144,754-240,144,754 , GRCh37 chr1: 240,308,054-240,308,054 PSMD2, FMN2, 1 more genes
    nsv4704198translocation1nstd195human GRCh37 chr3: 184,019,848-184,019,848 , GRCh38.p12 chr3: 184,302,060-184,302,060 , GRCh38.p12 chr1: 240,144,754-240,144,754 , GRCh37 chr1: 240,308,054-240,308,054 PSMD2, FMN2, 1 more genes
    nsv4674680copy number variation1nstd102humanPathogenic GRCh37 chr3: 169,617,690-190,593,854 , GRCh38.p12 chr3: 169,899,902-190,876,065 RNU6-1120P, LOC105374262, 323 more genes
    nsv4674171copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 183,789,584-186,034,649 , GRCh38.p12 chr3: 184,071,796-186,316,860 AP2M1, CLCN2, 54 more genes
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4108955copy number variation1nstd166human GRCh37.p13 chr3: 184,004,798-184,022,459 , GRCh38.p12 chr3: 184,287,010-184,304,671 EEF1AKMT4-ECE2, ECE2, 1 more genes
    nsv4100232copy number variation1nstd166human GRCh37.p13 chr3: 184,008,184-184,039,452 , GRCh38.p12 chr3: 184,290,396-184,321,664 ECE2, EIF4G1, 2 more genes
    nsv3922385copy number variation1nstd102humanPathogenic NCBI36 chr3: 177,369,007-199,329,651 , GRCh37 chr3: 175,886,313-197,845,254 , GRCh38 chr3: 176,168,525-198,118,383 LINC02053, RTP4, 414 more genes
    nsv3920662copy number variation1nstd102humanPathogenic NCBI36 chr3: 178,729,187-199,321,446 , GRCh37.p13 chr3: 177,246,493-197,837,049 , GRCh38.p12 chr3: 177,528,705-198,110,178 RN7SKP265, RPL24P6, 401 more genes
    nsv3919912copy number variation1nstd102humanLikely pathogenic NCBI36 chr3: 184,721,979-185,672,520 , GRCh37 chr3: 183,239,285-184,189,826 , GRCh38 chr3: 183,521,497-184,472,038 AP2M1, CLCN2, 42 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    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