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 1921

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096279copy number variation1nstd102humanPathogenic GRCh37 chr21: 34,648,881-34,655,566 , GRCh38.p12 chr21: 33,276,576-33,283,261 IL10RB
    nsv7096431copy number variation1nstd102humanPathogenic GRCh37 chr2: 9,663,358-9,666,393 , GRCh38.p12 chr2: 9,523,229-9,526,264 ADAM17
    nsv4682292copy number variation1nstd102humanPathogenic GRCh37 chr21: 34,648,881-34,649,078 , GRCh38.p12 chr21: 33,276,576-33,276,773 IL10RB
    nsv5564287copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 117,857,030-117,857,362 , GRCh38 chr11: 117,986,315-117,986,647 IL10RA
    nsv7095808copy number variation1nstd102humanUncertain significance GRCh37 chr21: 34,668,469-34,668,662 , GRCh38.p12 chr21: 33,296,164-33,296,357 IL10RB
    nsv3318287copy number variation1nstd157human GRCh37 chr16: 6,360,454-6,780,889 , GRCh38.p12 chr16: 6,310,453-6,730,888 RBFOX1
    nsv3317445copy number variation1nstd157human GRCh37 chr7: 61,738,085-61,886,130 , GRCh38.p12 chr16|NT_187383.1: 331,112-610,898 LOC102723945
    nsv3317793copy number variation1nstd157human GRCh37 chr4: 134,919,721-135,184,135 , GRCh38.p12 chr4: 133,998,566-134,262,980 PABPC4L
    nsv3317530copy number variation1nstd157human GRCh37 chr11: 48,677,994-48,923,129 , GRCh38.p12 chr11: 48,656,442-48,901,577 ANKRD33BP2
    nsv3318273copy number variation1nstd157human GRCh37 chr7: 8,956,393-9,193,798 , GRCh38.p12 chr7: 8,916,763-9,154,168 , GRCh38.p12 chr7|NW_019805493.1: 1-134,364 RPL9P19
    nsv3318329copy number variation1nstd157human GRCh37 chr2: 50,952,084-51,149,414 , GRCh38.p12 chr2: 50,724,946-50,922,276 NRXN1
    nsv3317205copy number variation3nstd157human GRCh37 chr4: 168,808,600-168,992,519 , GRCh38.p12 chr4: 167,887,449-168,071,368 LOC105377523
    nsv3318166copy number variation1nstd157human GRCh37 chr7: 145,928,594-146,110,464 , GRCh38.p12 chr7: 146,231,502-146,413,372 CNTNAP2
    nsv3318177copy number variation1nstd157human GRCh37 chr11: 81,841,736-82,023,512 , GRCh38.p12 chr11: 82,130,694-82,312,470 MIR4300HG
    nsv3318436copy number variation13nstd157human GRCh37 chr8: 137,682,484-137,862,080 , GRCh38.p12 chr8: 136,670,241-136,849,837 LINC02055
    nsv3317158copy number variation2nstd157human GRCh37 chr9: 12,094,891-12,272,490 , GRCh38.p12 chr9: 12,094,891-12,272,490 LOC105375976
    nsv3317586copy number variation1nstd157human GRCh37 chr2: 76,526,320-76,675,093 , GRCh38.p12 chr2: 76,299,194-76,447,967 RN7SKP203
    nsv3317457copy number variation1nstd157human GRCh37 chr7: 111,053,822-111,199,771 , GRCh38.p12 chr7: 111,413,766-111,559,715 IMMP2L
    nsv3318939copy number variation1nstd157human GRCh37 chr1: 189,337,997-189,469,295 , GRCh38.p12 chr1: 189,368,867-189,500,165 LOC105371657
    nsv3318890copy number variation1nstd157human GRCh37 chr4: 93,012,065-93,141,414 , GRCh38.p12 chr4: 92,090,914-92,220,263 PMPCAP1
    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