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Items: 1 to 20 of 283

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076079inversion1nstd229human GRCh38 chr16: 9,015,595-14,846,246 , GRCh37.p13 chr16: 9,109,452-14,940,103 LOC105371093, RNU6-633P, 100 more genes
    nsv6977322copy number variation1nstd229human GRCh38 chr16: 12,219,563-12,931,697 , GRCh37.p13 chr16: 12,313,420-13,025,554 LOC101927227, CPPED1, 8 more genes
    nsv6976957copy number variation1nstd229human GRCh38 chr16: 12,539,642-12,553,694 , GRCh37.p13 chr16: 12,633,499-12,647,551 SNX29, LOC105371085
    nsv6976710copy number variation1nstd229human GRCh38 chr16: 12,522,470-12,613,894 , GRCh37.p13 chr16: 12,616,327-12,707,751 SNX29, LOC105371085
    nsv6975921copy number variation1nstd229human GRCh38 chr16: 12,536,838-12,701,092 , GRCh37.p13 chr16: 12,630,695-12,794,949 SNX29, CPPED1, 2 more genes
    nsv6974023copy number variation1nstd229human GRCh38 chr16: 12,317,380-12,694,848 , GRCh37.p13 chr16: 12,411,237-12,788,705 LOC105371087, LOC105371088, 4 more genes
    nsv6973691copy number variation1nstd229human GRCh38 chr16: 12,556,201-12,563,400 , GRCh37.p13 chr16: 12,650,058-12,657,257 LOC105371085, SNX29
    nsv6968925copy number variation1nstd229human GRCh38 chr16: 12,510,571-12,658,582 , GRCh37.p13 chr16: 12,604,428-12,752,439 CPPED1, SNX29, 2 more genes
    nsv6967078copy number variation1nstd229human GRCh38 chr16: 12,542,567-12,557,598 , GRCh37.p13 chr16: 12,636,424-12,651,455 SNX29, LOC105371085
    nsv6966851copy number variation1nstd229human GRCh38 chr16: 12,565,804-12,628,664 , GRCh37.p13 chr16: 12,659,661-12,722,521 SNX29, LOC105371085
    nsv6966612copy number variation1nstd229human GRCh38 chr16: 12,356,212-12,756,742 , GRCh37.p13 chr16: 12,450,069-12,850,599 MIR4718, LOC101927227, 6 more genes
    nsv6965712copy number variation1nstd229human GRCh38 chr16: 12,163,201-12,587,300 , GRCh37.p13 chr16: 12,257,058-12,681,157 LOC101927227, LOC105371087, 2 more genes
    nsv6964793copy number variation1nstd229human GRCh38 chr16: 12,512,771-12,619,227 , GRCh37.p13 chr16: 12,606,628-12,713,084 SNX29, LOC105371085
    nsv6964320copy number variation1nstd229human GRCh38 chr16: 12,567,271-12,567,314 , GRCh37.p13 chr16: 12,661,128-12,661,171 LOC105371085, SNX29
    nsv6964078copy number variation1nstd229human GRCh38 chr16: 12,561,505-12,567,454 , GRCh37.p13 chr16: 12,655,362-12,661,311 LOC105371085, SNX29
    nsv6963816copy number variation1nstd229human GRCh38 chr16: 12,558,601-12,565,300 , GRCh37.p13 chr16: 12,652,458-12,659,157 LOC105371085, SNX29
    nsv6963525copy number variation1nstd229human GRCh38 chr16: 12,566,593-12,575,609 , GRCh37.p13 chr16: 12,660,450-12,669,466 SNX29, LOC105371085
    nsv6963094copy number variation1nstd229human GRCh38 chr16: 12,534,567-12,555,301 , GRCh37.p13 chr16: 12,628,424-12,649,158 LOC105371085, SNX29
    nsv6962318copy number variation1nstd229human GRCh38 chr16: 12,484,603-12,602,331 , GRCh37.p13 chr16: 12,578,460-12,696,188 LOC105371085, SNX29
    nsv6961860copy number variation1nstd229human GRCh38 chr16: 12,553,773-12,563,509 , GRCh37.p13 chr16: 12,647,630-12,657,366 LOC105371085, SNX29
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