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Items: 1 to 20 of 305

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148241copy number variation1nstd102humanPathogenic GRCh38 chr4: 79,123,548-99,457,773 , GRCh37.p13 chr4: 80,044,702-100,378,930 LOC105377327, LOC105377324, 214 more genes
    nsv7098835copy number variation1nstd102humanPathogenic GRCh37 chr4: 88,344,058-89,061,168 , GRCh38.p12 chr4: 87,422,906-88,140,016 SPARCL1, DSPP, 13 more genes
    nsv7057926inversion1nstd229human GRCh38 chr4: 87,164,841-87,871,077 , GRCh37.p13 chr4: 88,085,993-88,792,229 MIR5705, DSPP, 16 more genes
    nsv7054126inversion1nstd229human GRCh38 chr4: 87,165,000-87,871,044 , GRCh37.p13 chr4: 88,086,152-88,792,196 SCPPPQ1, LOC100129693, 16 more genes
    nsv7053656inversion1nstd229human GRCh38 chr4: 86,694,351-88,137,907 , GRCh37.p13 chr4: 87,615,504-89,059,059 KLHL8, GAPDHP60, 30 more genes
    nsv7050046inversion1nstd229human GRCh38 chr4: 85,500,769-88,545,032 , GRCh37.p13 chr4: 86,421,922-89,466,183 LOC105377326, NUDT9, 54 more genes
    nsv6757550copy number variation1nstd229human GRCh38 chr4: 87,495,127-87,529,042 , GRCh37.p13 chr4: 88,416,279-88,450,194 SPARCL1
    nsv6757218copy number variation1nstd229human GRCh38 chr4: 87,480,520-87,482,421 , GRCh37.p13 chr4: 88,401,672-88,403,573 SPARCL1
    nsv6754065copy number variation1nstd229human GRCh38 chr4: 87,478,151-87,481,019 , GRCh37.p13 chr4: 88,399,303-88,402,171 SPARCL1
    nsv6753982copy number variation1nstd229human GRCh38 chr4: 87,519,431-87,528,913 , GRCh37.p13 chr4: 88,440,583-88,450,065 SPARCL1
    nsv6752835copy number variation1nstd229human GRCh38 chr4: 87,493,701-87,494,600 , GRCh37.p13 chr4: 88,414,853-88,415,752 SPARCL1
    nsv6749121copy number variation1nstd229human GRCh38 chr4: 87,071,740-88,273,767 , GRCh37.p13 chr4: 87,992,892-89,194,919 RNU6-818P, DMP1, 29 more genes
    nsv6747056copy number variation1nstd229human GRCh38 chr4: 87,482,560-87,490,272 , GRCh37.p13 chr4: 88,403,712-88,411,424 SPARCL1
    nsv6745248copy number variation1nstd229human GRCh38 chr4: 87,495,128-87,499,520 , GRCh37.p13 chr4: 88,416,280-88,420,672 SPARCL1
    nsv6745105copy number variation1nstd229human GRCh38 chr4: 87,509,301-87,541,200 , GRCh37.p13 chr4: 88,430,453-88,462,352 SPARCL1
    nsv6742124copy number variation1nstd229human GRCh38 chr4: 87,474,279-87,536,390 , GRCh37.p13 chr4: 88,395,431-88,457,542 SPARCL1
    nsv6741302copy number variation1nstd229human GRCh38 chr4: 87,490,512-87,505,374 , GRCh37.p13 chr4: 88,411,664-88,426,526 SPARCL1
    nsv6739552copy number variation1nstd229human GRCh38 chr4: 87,526,147-87,526,237 , GRCh37.p13 chr4: 88,447,299-88,447,389 SPARCL1
    nsv6560212inversion1nstd223human GRCh38 chr4: 87,508,589-87,509,030 , GRCh37.p13 chr4: 88,429,741-88,430,182 SPARCL1
    nsv6557723inversion1nstd223human GRCh38 chr4: 87,472,000-87,472,776 , GRCh37.p13 chr4: 88,393,152-88,393,928 SPARCL1
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