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 12699

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3571105copy number variation1estd212human GRCh37 chr6: 62,486,662-62,927,082 , GRCh38.p12 chr6: 61,776,757-62,217,177 KHDRBS2
    esv3572838copy number variation1estd212human GRCh37 chr8: 76,610,056-76,961,841 , GRCh38.p12 chr8: 75,697,821-76,049,606 LOC105375906
    esv3569102copy number variation1estd212human GRCh37 chr3: 163,124,896-163,470,210 , GRCh38.p12 chr3: 163,407,108-163,752,422 RNU7-82P
    esv3580648copy number variation2estd212human GRCh37 chr13: 55,143,755-55,474,494 , GRCh38.p12 chr13: 54,569,620-54,900,359 LOC105370213
    esv3584087copy number variation1estd212human GRCh37 chr2: 137,920,766-138,225,635 , GRCh38.p12 chr2: 137,163,196-137,468,065 THSD7B
    esv3573133copy number variation1estd212human GRCh37 chr9: 11,645,688-11,941,917 , GRCh38.p12 chr9: 11,645,688-11,941,917 LOC101929446
    esv3573135copy number variation1estd212human GRCh37 chr9: 11,864,430-12,148,632 , GRCh38.p12 chr9: 11,864,430-12,148,632 LOC105375976
    esv3569696copy number variation2estd212human GRCh37 chr4: 134,918,953-135,191,179 , GRCh38.p12 chr4: 133,997,798-134,270,024 PABPC4L
    esv3583734copy number variation1estd212human GRCh37 chr2: 35,818,834-36,089,472 , GRCh38.p12 chr2: 35,593,768-35,864,406 MRPL50P1
    esv3573136copy number variation1estd212human GRCh37 chr9: 11,879,528-12,148,632 , GRCh38.p12 chr9: 11,879,528-12,148,632 LOC105375976
    esv3584052copy number variation1estd212human GRCh37 chr2: 126,806,753-127,054,351 , GRCh38.p12 chr2: 126,049,176-126,296,774 LINC01941
    esv3571666copy number variation1estd212human GRCh37 chr7: 15,334,035-15,575,393 , GRCh38.p12 chr7: 15,294,410-15,535,768 AGMO
    esv3569689copy number variation1estd212human GRCh37 chr4: 127,227,829-127,453,231 , GRCh38.p12 chr4: 126,306,674-126,532,076 LOC105377411
    esv3578322copy number variation1estd212human GRCh37 chr1: 189,320,336-189,537,683 , GRCh38.p12 chr1: 189,351,206-189,568,553 LOC105371657
    esv3583330copy number variation2estd212human GRCh37 chr19: 28,492,811-28,707,872 , GRCh38.p12 chr19: 28,001,904-28,216,965 LINC02987
    esv3578323copy number variation1estd212human GRCh37 chr1: 189,326,337-189,537,683 , GRCh38.p12 chr1: 189,357,207-189,568,553 LOC105371657
    esv3568771copy number variation1estd212human GRCh37 chr3: 60,067,512-60,277,128 , GRCh38.p12 chr3: 60,081,786-60,291,399 FHIT
    esv3569812copy number variation1estd212human GRCh37 chr4: 168,795,302-168,994,080 , GRCh38.p12 chr4: 167,874,151-168,072,929 LOC105377523
    esv3578964copy number variation1estd212human GRCh37 chr10: 68,356,145-68,551,219 , GRCh38.p12 chr10: 66,596,387-66,791,461 CTNNA3
    esv3578963copy number variation1estd212human GRCh37 chr10: 68,356,145-68,549,709 , GRCh38.p12 chr10: 66,596,387-66,789,951 CTNNA3
    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