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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143034copy number variation1nstd232human GRCh37.p13 chr17: 49,154,414-49,154,469 , GRCh38.p12 chr17: 51,077,053-51,077,108 SPAG9
    nsv7141397insertion1nstd232human GRCh37.p13 chr17: 49,119,015-49,119,015 , GRCh38.p12 chr17: 51,041,654-51,041,654 SPAG9
    nsv7139753insertion1nstd232human GRCh37.p13 chr17: 49,075,980-49,075,980 , GRCh38.p12 chr17: 50,998,619-50,998,619 SPAG9
    nsv7138256insertion1nstd232human GRCh37.p13 chr17: 49,079,205-49,079,205 , GRCh38.p12 chr17: 51,001,844-51,001,844 SPAG9
    nsv7061321inversion1nstd229human GRCh38 chr17: 51,097,572-51,099,946 , GRCh37.p13 chr17: 49,174,933-49,177,307 SPAG9
    nsv7058619inversion1nstd229human GRCh38 chr17: 49,389,100-51,159,770 , GRCh37.p13 chr17: 47,466,462-49,237,131 H1-9P, FLJ45513, 59 more genes
    nsv6996260copy number variation1nstd229human GRCh38 chr17: 50,954,408-50,964,541 , GRCh37.p13 chr17: 49,031,769-49,041,902 SPAG9
    nsv6991909copy number variation1nstd229human GRCh38 chr17: 51,102,015-51,105,981 , GRCh37.p13 chr17: 49,179,376-49,183,342 SPAG9
    nsv6991823copy number variation1nstd229human GRCh38 chr17: 50,979,441-50,979,539 , GRCh37.p13 chr17: 49,056,802-49,056,900 SPAG9
    nsv6990201copy number variation1nstd229human GRCh38 chr17: 51,051,171-51,051,675 , GRCh37.p13 chr17: 49,128,532-49,129,036 SPAG9
    nsv6987961copy number variation1nstd229human GRCh38 chr17: 51,076,989-51,077,041 , GRCh37.p13 chr17: 49,154,350-49,154,402 SPAG9
    nsv6986479copy number variation1nstd229human GRCh38 chr17: 51,121,219-51,156,678 , GRCh37.p13 chr17: 49,198,580-49,234,039 NME1, SPAG9, 1 more genes
    nsv6986384copy number variation1nstd229human GRCh38 chr17: 49,089,556-55,863,152 , GRCh37.p13 chr17: 47,166,918-53,940,513 LOC107985002, FAM117A, 107 more genes
    nsv6986065copy number variation1nstd229human GRCh38 chr17: 51,057,679-51,058,445 , GRCh37.p13 chr17: 49,135,040-49,135,806 SPAG9
    nsv6984487copy number variation1nstd229human GRCh38 chr17: 51,027,613-51,030,560 , GRCh37.p13 chr17: 49,104,974-49,107,921 SPAG9
    nsv6983431copy number variation1nstd229human GRCh38 chr17: 51,059,401-51,201,300 , GRCh37.p13 chr17: 49,136,762-49,278,661 NME2, NME1-NME2, 3 more genes
    nsv6982598copy number variation1nstd229human GRCh38 chr17: 50,992,183-51,176,536 , GRCh37.p13 chr17: 49,069,544-49,253,897 NME2, NME1-NME2, 3 more genes
    nsv6981423copy number variation1nstd229human GRCh38 chr17: 51,091,005-51,091,169 , GRCh37.p13 chr17: 49,168,366-49,168,530 SPAG9
    nsv6980184copy number variation1nstd229human GRCh38 chr17: 51,072,404-51,075,680 , GRCh37.p13 chr17: 49,149,765-49,153,041 SPAG9
    nsv6979566copy number variation1nstd229human GRCh38 chr17: 51,070,141-51,080,948 , GRCh37.p13 chr17: 49,147,502-49,158,309 SPAG9
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