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 105

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv4707895copy number variation1nstd195human GRCh37 chr3: 189,407,151-189,831,551 , GRCh38.p12 chr3: 189,689,362-190,113,762 TP63, P3H2, 2 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
    nsv4561014sequence alteration1nstd166human GRCh37.p13 chr3: 189,545,971-189,549,722 , GRCh38.p12 chr3: 189,828,182-189,831,933 TP63, MIR944
    nsv4436392copy number variation1nstd102humanPathogenic GRCh37 chr3: 188,386,566-197,838,262 , GRCh38.p12 chr3: 188,668,778-198,111,391 PPP1R2, GCNT1P3, 194 more genes
    nsv4366973copy number variation1nstd173human GRCh37 chr3: 189,445,224-189,561,865 , GRCh38.p12 chr3: 189,727,435-189,844,076 TP63, MIR944
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4102304copy number variation1nstd166human GRCh37.p13 chr3: 189,416,756-190,222,423 , GRCh38.p12 chr3: 189,698,967-190,504,634 TMEM207, RNU6-1109P, 8 more genes
    nsv3923340copy number variation1nstd102humanPathogenic GRCh38 chr3: 187,446,231-190,839,052 , GRCh37 chr3: 187,164,019-190,556,841 , NCBI36 chr3: 188,646,713-192,039,535 ENOPH1P1, LINC01991, 36 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
    nsv3920718copy number variation1nstd102humanPathogenic NCBI36 chr3: 188,646,713-196,231,151 , GRCh37 chr3: 187,164,019-194,749,862 , GRCh38 chr3: 187,446,231-195,029,133 LOC105374283, MIR944, 105 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
    nsv3920607copy number variation1nstd102humanPathogenic NCBI36 chr3: 187,082,628-197,946,692 , GRCh37.p13 chr3: 185,599,934-196,462,295 , GRCh38.p12 chr3: 185,882,146-196,735,424 FGF12, RFC4, 212 more genes
    nsv3920067copy number variation1nstd102humanPathogenic GRCh38 chr3: 189,265,371-198,110,178 , NCBI36 chr3: 190,465,854-199,321,446 , GRCh37 chr3: 188,983,160-197,837,049 OSTN-AS1, ACAP2, 188 more genes
    nsv3919035copy number variation1nstd102humanLikely benign NCBI36 chr3: 190,418,985-191,290,326 , GRCh37 chr3: 188,936,291-189,807,632 , GRCh38 chr3: 189,218,502-190,089,843 TP63, TPRG1, 5 more genes
    nsv3918982copy number variation1nstd102humanPathogenic GRCh37 chr3: 167,885,356-197,837,049 , NCBI36 chr3: 169,368,050-199,321,446 , GRCh38 chr3: 168,167,568-198,110,178 EIF4G1, LOC105374248, 515 more genes
    nsv3918981copy number variation1nstd102humanPathogenic GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446 LINC02614, LINC02054, 1469 more genes
    nsv3918718copy number variation1nstd102humanPathogenic GRCh37 chr3: 186,482,937-194,130,145 , NCBI36 chr3: 187,965,631-195,611,434 , GRCh38 chr3: 186,765,148-194,409,416 TPRG1-AS1, GCNT1P3, 114 more genes
    nsv3918692copy number variation1nstd102humanPathogenic GRCh38 chr3: 147,521,892-198,096,565 , GRCh37 chr3: 147,239,679-197,823,436 , NCBI36 chr3: 148,722,369-199,307,833 LOC105374179, LINC02038, 785 more genes
    nsv3918149copy number variation1nstd102humanPathogenic GRCh37 chr3: 155,836,230-197,851,986 , GRCh38 chr3: 156,118,441-198,125,115 , NCBI36 chr3: 157,318,924-199,336,383 LINC02031, PCBP2P4, 647 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