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
    esv2763832copy number variation300estd203human NCBI36 chr4: 9,802,525-9,848,395 , GRCh37.p13 chr4: 10,193,427-10,239,297 , GRCh38.p12 chr4: 10,191,803-10,237,673 LOC100129344
    esv2763673copy number variation70estd203human NCBI36 chr20: 52,070,481-52,101,533 , GRCh37.p13 chr20: 52,637,074-52,668,126 , GRCh38.p12 chr20: 54,020,535-54,051,587 BCAS1
    esv2761410copy number variation88estd203human NCBI36 chr1: 167,500,598-167,522,026 , GRCh37.p13 chr1: 169,233,974-169,255,402 , GRCh38.p12 chr1: 169,264,736-169,286,164 NME7
    esv2763902copy number variation115estd203human NCBI36 chr10: 24,412,311-24,421,030 , GRCh37.p13 chr10: 24,372,305-24,381,024 , GRCh38.p12 chr10: 24,083,376-24,092,095 KIAA1217
    esv2760988copy number variation56estd203human NCBI36 chr12: 98,315,274-98,322,865 , GRCh37.p13 chr12: 99,791,143-99,798,734 , GRCh38.p12 chr12: 99,397,365-99,404,956 ANKS1B
    esv2762165copy number variation148estd203human NCBI36 chr16: 76,905,239-77,100,500 , GRCh37.p13 chr16: 78,347,738-78,542,999 , GRCh38.p12 chr16: 78,313,841-78,509,102 WWOX, LSM3P5
    esv2764074copy number variation121estd203human NCBI36 chr8: 39,344,897-39,523,161 , GRCh37.p13 chr8: 39,225,740-39,404,004 , GRCh38.p12 chr8: 39,368,221-39,546,485 ADAM3A, ADAM5
    esv2760788copy number variation68estd203human NCBI36 chr12: 2,102,418-2,140,552 , GRCh37.p13 chr12: 2,232,157-2,270,291 , GRCh38.p12 chr12: 2,122,991-2,161,125 , GRCh38.p12 chr12|NW_018654718.1: 465,135-503,269 CACNA1C, LOC107984131
    esv2760399copy number variation143estd203human NCBI36 chr11: 4,923,952-4,943,583 , GRCh37.p13 chr11: 4,967,376-4,987,007 , GRCh38.p12 chr11: 4,946,146-4,965,777 OR51A4, OR51A2
    esv2763928copy number variation116estd203human NCBI36 chr5: 12,853,889-12,945,132 , GRCh37.p13 chr5: 12,800,889-12,892,132 , GRCh38.p12 chr5: 12,800,777-12,892,020 LINC01194, LOC105374657, 1 more genes
    esv2763812copy number variation96estd203human GRCh38.p12 chr4: 68,494,770-68,727,128 , GRCh37.p13 chr4: 69,360,488-69,592,846 , NCBI36 chr4: 69,043,083-69,378,740 UGT2B15, UGT2B17, 6 more genes
    esv2762399copy number variation6estd203human NCBI36 chr17: 30,700,619-30,792,312 , GRCh37.p13 chr17: 33,676,506-33,768,199 , GRCh38.p12 chr17: 35,349,487-35,441,180 SLFN12, SLFN11, 4 more genes
    esv2761755copy number variation405estd203human NCBI36 chr15: 18,276,341-21,038,987 , GRCh37.p13 chr15: 20,016,328-23,487,546 , GRCh38.p12 chr15: 19,811,075-22,308,242 OR11K1P, LOC283804, 99 more genes
    esv2764166copy number variation266estd203human NCBI36 chr9: 43,255,666-44,936,428 , GRCh37.p13 chr9: 43,315,670-44,996,432 , GRCh38.p12 chr9: 41,912,139-42,974,549 SPATA31A6, ADGRF5P2, 30 more genes
    esv2764095copy number variation266estd203human NCBI36 chr8: 11,914,604-12,622,461 , GRCh37.p13 chr8: 11,877,195-12,578,090 , GRCh38.p12 chr8: 12,019,686-12,720,581 OR7E15P, FAM86B1, 38 more genes
    esv2760444copy number variation76estd203human NCBI36 chr11: 81,175,086-81,226,406 , GRCh37.p13 chr11: 81,497,438-81,548,758 , GRCh38.p12 chr11: 81,786,396-81,837,716 0
    esv2763864copy number variation30estd203human NCBI36 chr5: 8,754,366-8,802,776 , GRCh37.p13 chr5: 8,701,366-8,749,776 , GRCh38.p12 chr5: 8,701,254-8,749,664 0
    esv2763788copy number variation27estd203human NCBI36 chr4: 161,254,096-161,290,239 , GRCh37.p13 chr4: 161,034,646-161,070,789 , GRCh38.p12 chr4: 160,113,494-160,149,637 0
    esv2763828copy number variation173estd203human GRCh38.p12 chr4: 69,248,737-69,453,762 , GRCh37.p13 chr4: 70,114,455-70,319,480 , NCBI36 chr4: 70,149,044-70,354,069 UGT2B28, UGT2B25P, 6 more genes
    esv2760311copy number variation127estd203human NCBI36 chr11: 55,117,937-55,260,932 , GRCh37.p13 chr11: 55,361,361-55,504,356 , GRCh38.p12 chr11: 55,593,885-55,736,880 OR5D3P, OR5D2P, 6 more genes
    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