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 23

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3317580copy number variation32nstd157human GRCh37 chr7: 156,387,296-156,394,307 , GRCh38.p12 chr7: 156,594,602-156,601,613 RNF32-DT
    nsv3317944copy number variation11nstd157human GRCh37 chr8: 36,070,428-36,076,949 , GRCh38.p12 chr8: 36,212,910-36,219,431 LOC105379371
    nsv3318029copy number variation27nstd157human GRCh37 chr18: 41,976,831-41,982,102 , GRCh38.p12 chr18: 44,396,866-44,402,137 LINC01478
    nsv3318609copy number variation1nstd157human GRCh37 chr3: 4,310,636-4,340,847 , GRCh38.p12 chr3: 4,268,952-4,299,163 SUMF1
    nsv3317222copy number variation1nstd157human GRCh38.p12 chr15: 58,429,451-58,438,372 , GRCh37 chr15: 58,721,650-58,730,571 LIPC, LIPC-AS1
    nsv3318734copy number variation11nstd157human GRCh38.p12 chr19: 53,015,494-53,045,697 , GRCh37 chr19: 53,518,747-53,548,950 ERVV-1, ERVV-2
    nsv3317318copy number variation3nstd157human GRCh38.p12 chr22: 42,512,492-42,554,027 , GRCh37 chr22: 42,908,498-42,950,033 RRP7A, SERHL, 1 more genes
    nsv3318429copy number variation1nstd157human GRCh38.p12 chr14: 99,928,476-99,951,505 , GRCh37 chr14: 100,394,813-100,417,842 EML1, LOC102724682, 1 more genes
    nsv3317868copy number variation3nstd157human GRCh37 chr16: 32,257,633-32,642,384 , GRCh38.p12 chr16: 32,246,312-32,631,063 ABCD1P3, LOC390705, 8 more genes
    nsv3318033copy number variation1nstd157human GRCh37 chr4: 11,305,539-11,330,277 , GRCh38.p12 chr4: 11,303,915-11,328,653 0
    nsv3317075copy number variation4nstd157human GRCh37 chr3: 175,887,314-175,909,890 , GRCh38.p12 chr3: 176,169,526-176,192,102 , GRCh38.p12 chr3|NW_019805488.1: 54,037-76,613 0
    nsv3318929copy number variation2nstd157human GRCh37 chr4: 189,249,073-189,267,822 , GRCh38.p12 chr4: 188,327,919-188,346,668 0
    nsv3317289copy number variation24nstd157human GRCh37 chr9: 24,502,737-24,518,795 , GRCh38.p12 chr9: 24,502,739-24,518,797 0
    nsv3318427copy number variation34nstd157human GRCh37 chr11: 81,501,218-81,517,261 , GRCh38.p12 chr11: 81,790,176-81,806,219 0
    nsv3318039copy number variation18nstd157human GRCh37 chr13: 58,589,893-58,599,174 , GRCh38.p12 chr13: 58,015,759-58,025,040 0
    nsv3318502copy number variation31nstd157human GRCh37 chr9: 78,004,378-78,011,616 , GRCh38.p12 chr9: 75,389,462-75,396,700 0
    nsv3317750copy number variation5nstd157human GRCh37 chr6: 118,077,577-118,084,347 , GRCh38.p12 chr6: 117,756,414-117,763,184 0
    nsv3317208copy number variation8nstd157human GRCh37 chr2: 8,130,069-8,136,251 , GRCh38.p12 chr2: 7,989,938-7,996,120 0
    nsv3317426copy number variation1nstd157human GRCh37 chr6: 26,612,363-26,617,623 , GRCh38.p12 chr6: 26,612,135-26,617,395 0
    nsv3318900copy number variation17nstd157human GRCh37 chr7: 86,940,652-86,945,816 , GRCh38.p12 chr7: 87,311,336-87,316,500 0
    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