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 857

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3318353copy number variation3nstd157human GRCh37 chr16: 79,260,765-79,273,682 , GRCh38.p12 chr16: 79,226,868-79,239,785 MAF
    nsv3318206copy number variation5nstd157human GRCh37 chr6: 161,268,770-161,277,436 , GRCh38.p12 chr6: 160,847,738-160,856,404 LOC107986665
    nsv3318084copy number variation1nstd157human GRCh37 chr3: 165,520,831-165,875,790 , GRCh38.p12 chr3: 165,803,043-166,158,002 BCHE
    nsv3318359copy number variation1nstd157human GRCh37 chr11: 133,008,293-133,268,476 , GRCh38.p12 chr11: 133,138,398-133,398,581 OPCML
    nsv3317540copy number variation1nstd157human GRCh37 chr11: 50,325,741-50,525,694 , GRCh38.p12 chr11: 50,366,570-50,566,523 LOC646813
    nsv3318654copy number variation3nstd157human GRCh37 chr7: 100,967,084-101,135,490 , GRCh38.p12 chr7: 101,323,803-101,492,209 COL26A1
    nsv3317666copy number variation21nstd157human GRCh37 chr21: 10,715,343-10,883,039 , GRCh38.p12 chr21: 10,629,418-10,797,114 IGHV1OR21-1
    nsv3318781copy number variation1nstd157human GRCh37 chr3: 140,785,834-140,909,061 , GRCh38.p12 chr3: 141,066,992-141,190,219 SPSB4
    nsv3318094copy number variation1nstd157human GRCh37 chr8: 91,293,849-91,414,539 , GRCh38.p12 chr8: 90,281,621-90,402,311 LINC00534
    nsv3317667copy number variation1nstd157human GRCh37 chr14: 44,821,980-44,930,894 , GRCh38.p12 chr14: 44,352,777-44,461,691 LINC02277
    nsv3318341copy number variation1nstd157human GRCh37 chr1: 104,546,820-104,650,090 , GRCh38.p12 chr1: 104,004,198-104,107,468 THAP3P1
    nsv3318810copy number variation1nstd157human GRCh37 chr5: 106,271,054-106,365,839 , GRCh38.p12 chr5: 106,935,353-107,030,138 LINC01950
    nsv3318163copy number variation1nstd157human GRCh37 chr3: 118,730,933-118,822,359 , GRCh38.p12 chr3: 119,012,086-119,103,512 IGSF11
    nsv3318905copy number variation1nstd157human GRCh37 chr3: 118,730,933-118,821,415 , GRCh38.p12 chr3: 119,012,086-119,102,568 IGSF11
    nsv3317715copy number variation1nstd157human GRCh37 chr20: 12,802,070-12,889,314 , GRCh38.p12 chr20: 12,821,422-12,908,666 LINC01722
    nsv3317847copy number variation1nstd157human GRCh37 chr10: 66,851,191-66,933,364 , GRCh38.p12 chr10: 65,091,433-65,173,606 MYL6P3
    nsv3318843copy number variation1nstd157human GRCh37 chr13: 108,328,479-108,410,359 , GRCh38.p12 chr13: 107,676,131-107,758,011 NALF1
    nsv3317420copy number variation1nstd157human GRCh37 chr17: 9,989,998-10,071,868 , GRCh38.p12 chr17: 10,086,681-10,168,551 GAS7
    nsv3318511copy number variation4nstd157human GRCh37 chr3: 126,683,523-126,761,939 , GRCh38.p12 chr3: 126,964,680-127,043,096 PLXNA1
    nsv3318534copy number variation1nstd157human GRCh37 chr3: 21,258,435-21,336,755 , GRCh38.p12 chr3: 21,216,943-21,295,263 LOC105376988
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    Recent activity

    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center