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 83

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3118102copy number variation23nstd145human GRCh37 chr14: 41,610,669-41,668,279 , GRCh38.p12 chr14: 41,141,466-41,199,076 LINC02315
    nsv3118081copy number variation72nstd145human GRCh37 chr7: 141,766,533-141,793,377 , GRCh38.p12 chr7|NT_187562.1: 28,613-55,457 , GRCh38.p12 chr7: 142,066,733-142,093,577 MGAM
    nsv3117809copy number variation152nstd145human GRCh37 chr20: 1,561,593-1,584,273 , GRCh38.p12 chr20: 1,580,947-1,603,627 SIRPB1
    nsv3113671copy number variation1nstd145human GRCh37 chr8: 17,573,501-17,588,754 , GRCh38.p12 chr8: 17,715,992-17,731,245 MTUS1
    nsv3114057copy number variation160nstd145human GRCh37 chr19: 52,134,789-52,148,550 , GRCh38.p12 chr19: 51,631,536-51,645,297 SIGLEC14
    nsv3112094copy number variation94nstd145human GRCh37 chr7: 133,785,285-133,797,218 , GRCh38.p12 chr7: 134,100,532-134,112,465
    nsv3117489copy number variation5nstd145human GRCh37 chr1: 231,535,550-231,545,954 , GRCh38.p12 chr1: 231,399,804-231,410,208 EGLN1
    nsv3113383copy number variation199nstd145human GRCh37 chr3: 192,875,554-192,885,008 , GRCh38.p12 chr3: 193,157,765-193,167,219 VEZF1P1
    nsv3113216copy number variation2nstd145human GRCh37 chr8: 51,031,100-51,039,215 , GRCh38.p12 chr8: 50,118,540-50,126,655 SNTG1
    nsv3117623copy number variation16nstd145human GRCh37 chr1: 35,104,240-35,112,001 , GRCh38.p12 chr1: 34,638,639-34,646,400 LOC105378641
    nsv3115987copy number variation16nstd145human GRCh37 chr18: 66,749,133-66,756,183 , GRCh38.p12 chr18: 69,081,896-69,088,946 CCDC102B
    nsv3117297copy number variation80nstd145human GRCh37 chr7: 154,392,836-154,399,317 , GRCh38.p12 chr7: 154,601,126-154,607,607 DPP6
    nsv3112895copy number variation76nstd145human GRCh37 chr12: 43,020,941-43,027,293 , GRCh38.p12 chr12: 42,627,139-42,633,491 LINC02402
    nsv3114208copy number variation43nstd145human GRCh37 chr3: 189,364,561-189,370,847 , GRCh38.p12 chr3: 189,646,772-189,653,058 TP63
    nsv3113554copy number variation1nstd145human GRCh37 chr6: 169,463,891-169,469,493 , GRCh38.p12 chr6: 169,063,796-169,069,398 LOC102724357
    nsv3115419copy number variation1nstd145human GRCh37 chr20: 54,282,598-54,288,123 , GRCh38.p12 chr20: 55,707,542-55,713,067 LOC107984001
    nsv3112349copy number variation62nstd145human GRCh37 chr4: 107,056,600-107,062,092 , GRCh38.p12 chr4: 106,135,443-106,140,935 TBCK
    nsv3117385copy number variation76nstd145human GRCh37 chr7: 110,182,897-110,188,346 , GRCh38.p12 chr7: 110,542,840-110,548,289 LOC105375451
    nsv3117711copy number variation27nstd145human GRCh37 chr3: 22,280,757-22,285,798 , GRCh38.p12 chr3: 22,239,265-22,244,306 ZNF385D
    nsv3114178copy number variation107nstd145human GRCh37 chr6: 53,928,991-53,933,879 , GRCh38.p12 chr6: 54,064,193-54,069,081 MLIP
    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