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Items: 1 to 20 of 375

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980400copy number variation1nstd102humanLikely benign GRCh37 chr9: 139,325,718-139,326,259 , GRCh38 chr9: 136,431,266-136,431,807 INPP5E
    nsv5919819copy number variation1nstd209human GRCh38 chr9: 136,433,842-136,433,916 , GRCh37.p13 chr9: 139,328,294-139,328,368 INPP5E
    nsv5673813copy number variation1nstd102humanLikely benign GRCh37 chr9: 139,326,135-139,326,259 , GRCh38 chr9: 136,431,683-136,431,807 INPP5E
    nsv5639247insertion1nstd207human GRCh38 chr9: 136,431,682-136,431,682 , GRCh37.p13 chr9: 139,326,134-139,326,134 INPP5E
    nsv5634387insertion1nstd207human GRCh38 chr9: 136,431,770-136,431,770 , GRCh37.p13 chr9: 139,326,222-139,326,222 INPP5E
    nsv5602278copy number variation1nstd207human GRCh38 chr9: 136,431,432-136,431,722 , GRCh37.p13 chr9: 139,325,884-139,326,174 INPP5E
    nsv5589806copy number variation1nstd207human GRCh38 chr9: 136,431,266-136,431,347 , GRCh37.p13 chr9: 139,325,718-139,325,799 INPP5E
    nsv5564514copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,315,643-139,465,759 , GRCh38.p12 chr9: 136,421,191-136,571,307 NOTCH1, SEC16A, 6 more genes
    nsv5564455copy number variation1nstd102humanUncertain significance GRCh37 chr9: 139,297,240-139,572,028 , GRCh38.p12 chr9: 136,402,788-136,677,576 LOC105376325, NOTCH1, 14 more genes
    nsv5492575copy number variation1nstd206human GRCh38 chr9: 136,431,210-136,431,831 , GRCh37.p13 chr9: 139,325,662-139,326,283 INPP5E
    nsv5486937copy number variation1nstd206human GRCh38 chr9: 136,433,863-136,458,547 , GRCh37.p13 chr9: 139,328,315-139,352,999 SEC16A, INPP5E
    nsv5381762copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,284,464-141,018,984 , GRCh38.p12 chr9: 136,390,012-138,124,532 ARRDC1, SETP5, 101 more genes
    nsv5254857copy number variation1nstd204human GRCh38.p13 chr9: 136,423,301-136,428,000 , GRCh37.p13 chr9: 139,317,753-139,322,452 INPP5E, PMPCA
    nsv5246206copy number variation1nstd204human GRCh38.p13 chr9: 136,043,001-136,766,200 , GRCh37.p13 chr9: 138,934,847-139,660,652 MIR4674, TMEM250, 37 more genes
    nsv5244105copy number variation1nstd204human GRCh38.p13 chr9: 136,423,503-136,427,902 , GRCh37.p13 chr9: 139,317,955-139,322,354 INPP5E, PMPCA
    nsv5241174copy number variation1nstd204human GRCh38.p13 chr9: 136,431,201-136,431,800 , GRCh37.p13 chr9: 139,325,653-139,326,252 INPP5E
    nsv4985867copy number variation1nstd200human GRCh38 chr9: 136,433,863-136,458,547 , GRCh37.p13 chr9: 139,328,315-139,352,999 SEC16A, INPP5E
    nsv4985863copy number variation1nstd200human GRCh38 chr9: 136,239,913-136,449,610 , GRCh37.p13 chr9: 139,131,759-139,344,062 CCDC187, SNAPC4, 9 more genes
    nsv4973354copy number variation1nstd200human GRCh38 chr9: 136,425,512-136,427,416 , GRCh37.p13 chr9: 139,319,964-139,321,868 INPP5E
    nsv4768352copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,018,777-141,018,984 , GRCh38.p12 chr9: 136,126,931-138,124,532 MIR6722, EXD3, 108 more genes
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