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Items: 1 to 20 of 1590

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6126046insertion1nstd186human GRCh37 chr4: 79,159,505-79,159,505 , GRCh38.p12 chr4: 78,238,351-78,238,351 FRAS1
    nsv6115016mobile element insertion1nstd186human GRCh37 chr4: 79,243,725-79,243,776 , GRCh38.p12 chr4: 78,322,571-78,322,622 FRAS1
    nsv6114943mobile element insertion1nstd186human GRCh37 chr4: 79,359,159-79,359,159 , GRCh38.p12 chr4: 78,438,005-78,438,005 FRAS1
    nsv5961784insertion1nstd209human GRCh38 chr4: 78,401,812-78,401,812 , GRCh37.p13 chr4: 79,322,966-79,322,966 FRAS1
    nsv5955174insertion1nstd209human GRCh38 chr4: 78,438,005-78,438,005 , GRCh37.p13 chr4: 79,359,159-79,359,159 FRAS1
    nsv5952012insertion1nstd209human GRCh38 chr4: 78,483,769-78,483,769 , GRCh37.p13 chr4: 79,404,923-79,404,923 FRAS1
    nsv5951189insertion1nstd209human GRCh38 chr4: 78,368,280-78,368,280 , GRCh37.p13 chr4: 79,289,434-79,289,434 FRAS1
    nsv5950350insertion1nstd209human GRCh38 chr4: 78,238,351-78,238,351 , GRCh37.p13 chr4: 79,159,505-79,159,505 FRAS1
    nsv5950150insertion1nstd209human GRCh38 chr4: 78,249,064-78,249,064 , GRCh37.p13 chr4: 79,170,218-79,170,218 FRAS1
    nsv5949613insertion1nstd209human GRCh38 chr4: 78,065,081-78,065,081 , GRCh37.p13 chr4: 78,986,235-78,986,235 FRAS1
    nsv5947589insertion1nstd209human GRCh38 chr4: 78,450,993-78,450,993 , GRCh37.p13 chr4: 79,372,147-79,372,147 FRAS1
    nsv5906449copy number variation1nstd209human GRCh38 chr4: 78,140,639-78,140,712 , GRCh37.p13 chr4: 79,061,793-79,061,866 FRAS1
    nsv5903710copy number variation1nstd209human GRCh38 chr4: 77,961,607-78,271,368 , GRCh37.p13 chr4: 78,882,761-79,192,522 FRAS1, HNRNPA1P56, 3 more genes
    nsv5902102copy number variation1nstd209human GRCh38 chr4: 78,129,505-78,129,574 , GRCh37.p13 chr4: 79,050,659-79,050,728 FRAS1
    nsv5901743copy number variation1nstd209human GRCh38 chr4: 78,420,484-78,420,586 , GRCh37.p13 chr4: 79,341,638-79,341,740 FRAS1
    nsv5901581copy number variation1nstd209human GRCh38 chr4: 78,470,797-78,471,483 , GRCh37.p13 chr4: 79,391,951-79,392,637 FRAS1
    nsv5899843copy number variation1nstd209human GRCh38 chr4: 78,167,295-78,173,047 , GRCh37.p13 chr4: 79,088,449-79,094,201 FRAS1
    nsv5899777copy number variation1nstd209human GRCh38 chr4: 78,347,966-78,354,040 , GRCh37.p13 chr4: 79,269,120-79,275,194 FRAS1
    nsv5899678copy number variation1nstd209human GRCh38 chr4: 78,334,517-78,337,064 , GRCh37.p13 chr4: 79,255,671-79,258,218 FRAS1
    nsv5899441copy number variation1nstd209human GRCh38 chr4: 78,091,928-78,092,032 , GRCh37.p13 chr4: 79,013,082-79,013,186 FRAS1
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