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Items: 1 to 20 of 191

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138277insertion1nstd232human GRCh37.p13 chr17: 49,238,634-49,238,634 , GRCh38.p12 chr17: 51,161,273-51,161,273 NME1, NME1-NME2
    nsv7058619inversion1nstd229human GRCh38 chr17: 49,389,100-51,159,770 , GRCh37.p13 chr17: 47,466,462-49,237,131 H1-9P, FLJ45513, 59 more genes
    nsv6989494copy number variation1nstd229human GRCh38 chr17: 51,143,843-51,151,568 , GRCh37.p13 chr17: 49,221,204-49,228,929 NME1, NME1-NME2
    nsv6987634copy number variation1nstd229human GRCh38 chr17: 51,166,301-51,169,500 , GRCh37.p13 chr17: 49,243,662-49,246,861 NME1-NME2, NME2
    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
    nsv6984914copy number variation1nstd229human GRCh38 chr17: 51,152,468-51,154,394 , GRCh37.p13 chr17: 49,229,829-49,231,755 NME1, NME1-NME2
    nsv6984251copy number variation1nstd229human GRCh38 chr17: 51,152,720-51,221,763 , GRCh37.p13 chr17: 49,230,081-49,299,124 MBTD1, NME2, 2 more genes
    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
    nsv6594178inversion1nstd223human GRCh38 chr17: 51,170,256-51,170,526 , GRCh37.p13 chr17: 49,247,617-49,247,887 NME1-NME2, NME2
    nsv6580702inversion1nstd223human GRCh38 chr17: 51,162,932-51,163,522 , GRCh37.p13 chr17: 49,240,293-49,240,883 NME1-NME2
    nsv6531238copy number variation1nstd223human GRCh38 chr17: 51,170,240-51,171,066 , GRCh37.p13 chr17: 49,247,601-49,248,427 NME2, NME1-NME2
    nsv6523040copy number variation1nstd223human GRCh38 chr17: 51,158,592-51,160,176 , GRCh37.p13 chr17: 49,235,953-49,237,537 NME1, NME1-NME2
    nsv6519380copy number variation1nstd223human GRCh38 chr17: 51,167,451-51,169,221 , GRCh37.p13 chr17: 49,244,812-49,246,582 NME1-NME2, NME2
    nsv6273960copy number variation1nstd214human GRCh38 chr17: 51,151,991-51,152,070 , GRCh37.p13 chr17: 49,229,352-49,229,431 NME1-NME2, NME1
    nsv6133068copy number variation1nstd213human GRCh37 chr17: 49,110,000-49,280,001 , GRCh38.p12 chr17: 51,032,639-51,202,640 NME1, NME2, 3 more genes
    nsv5701410mobile element insertion1nstd211human GRCh38 chr17: 51,157,577-51,157,577 , GRCh37.p13 chr17: 49,234,938-49,234,938 NME1, NME1-NME2
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5553539insertion1nstd206human GRCh38 chr17: 51,157,527-51,157,577 , GRCh37.p13 chr17: 49,234,888-49,234,938 NME1, NME1-NME2
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