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Items: 1 to 20 of 376296

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6752150copy number variation1nstd229human GRCh38 chr4: 179,256,128-180,403,825 , GRCh37.p13 chr4: 180,177,282-181,324,978 LOC105377567
    nsv6883374copy number variation1nstd229human GRCh38 chr10: 54,873,684-55,577,081 , GRCh37.p13 chr10: 56,633,444-57,336,841 PCDH15
    nsv7002843copy number variation1nstd229human GRCh38 chr18: 29,551,903-30,222,824 , GRCh37.p13 chr18: 27,131,868-27,802,789 LOC105372045
    nsv6814235copy number variation1nstd229human GRCh38 chr6: 103,059,801-103,708,200 , GRCh37.p13 chr6: 103,507,676-104,156,075 LOC105377916
    nsv6776614copy number variation1nstd229human GRCh38 chr5: 62,924,623-63,568,423 , GRCh37.p13 chr5: 62,220,450-62,864,250 LOC100420027
    nsv6735908copy number variation1nstd229human GRCh38 chr4: 59,552,266-60,173,231 , GRCh37.p13 chr4: 60,417,984-61,038,949 RNU6-1325P
    nsv6932741copy number variation1nstd229human GRCh38 chr12: 60,715,785-61,309,407 , GRCh37.p13 chr12: 61,109,566-61,703,188 PGBD3P1
    nsv6808777copy number variation1nstd229human GRCh38 chr6: 123,950,834-124,542,292 , GRCh37.p13 chr6: 124,271,979-124,863,438 NKAIN2
    nsv6833837copy number variation1nstd229human GRCh38 chr7: 69,809,078-70,386,577 , GRCh37.p13 chr7: 69,274,064-69,851,563 AUTS2
    nsv6774409copy number variation1nstd229human GRCh38 chr5: 120,882,817-121,442,939 , GRCh37.p13 chr5: 120,218,512-120,778,634 LOC102467226
    nsv7081755copy number variation1nstd229human GRCh38 chrX: 94,919,950-95,467,853 , GRCh37.p13 chrX: 94,174,949-94,722,852 MIR548M
    nsv6662913copy number variation1nstd229human GRCh38 chr2: 58,511,979-59,053,496 , GRCh37.p13 chr2: 58,739,114-59,280,631 LINC01122
    nsv6868033copy number variation1nstd229human GRCh38 chr8: 136,545,719-137,083,811 , GRCh37.p13 chr8: 137,557,962-138,096,054 LINC02055
    nsv6823724copy number variation1nstd229human GRCh38 chr7: 145,691,599-146,226,417 , GRCh37.p13 chr7: 145,388,692-145,923,509 CNTNAP2
    nsv6793044copy number variation1nstd229human GRCh38 chr6: 66,150,634-66,674,395 , GRCh37.p13 chr6: 66,860,527-67,384,288 LOC105377841
    nsv6827413copy number variation1nstd229human GRCh38 chr7: 125,695,563-126,215,791 , GRCh37.p13 chr7: 125,335,617-125,855,845 LOC105375487
    nsv6751515copy number variation1nstd229human GRCh38 chr4: 63,628,301-64,143,800 , GRCh37.p13 chr4: 64,494,019-65,009,518 LOC105377254
    nsv6759885copy number variation1nstd229human GRCh38 chr5: 84,604,501-85,119,100 , GRCh37.p13 chr5: 83,900,319-84,414,918 PPIAP79
    nsv6719194copy number variation1nstd229human GRCh38 chr4: 34,139,665-34,649,409 , GRCh37.p13 chr4: 34,141,287-34,651,031 LINC02484
    nsv6743632copy number variation1nstd229human GRCh38 chr4: 62,744,909-63,253,543 , GRCh37.p13 chr4: 63,610,627-64,119,261 EXOC5P1
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