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Items: 1 to 20 of 387

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146354insertion1nstd232human GRCh37.p13 chr17: 66,227,556-66,227,556 , GRCh38.p12 chr17: 68,231,415-68,231,415 AMZ2
    nsv7077537inversion1nstd229human GRCh38 chr17: 64,968,697-68,255,761 , GRCh37.p13 chr17: 62,964,815-65,936,105 SNORA38B, PRKCA-AS1, 52 more genes
    nsv7070446inversion1nstd229human GRCh38 chr17: 65,003,854-68,220,374 , GRCh37.p13 chr17: 62,999,972-65,936,105 SH3GL1P3, AXIN2, 51 more genes
    nsv7068396inversion1nstd229human GRCh38 chr17: 68,158,444-69,264,023 , GRCh37.p13 chr17: 66,324,471-67,260,164 ABCA9, MIR4524A, 21 more genes
    nsv7064125inversion1nstd229human GRCh38 chr17: 68,059,302-68,471,860 , GRCh37.p13 chr17: 66,055,418-66,324,470 , GRCh37.p13 chr17|NW_003871088.1: 119,313-388,340 TRUND-NNN5-1, LRRC37A16P, 12 more genes
    nsv7060872inversion1nstd229human GRCh38 chr17: 68,057,734-68,472,338 , GRCh37.p13 chr17: 66,053,850-66,324,470 , GRCh37.p13 chr17|NW_003871088.1: 117,745-388,340 FBXO36P1, LRRC37A16P, 12 more genes
    nsv7059173inversion1nstd229human GRCh38 chr17: 65,003,895-68,220,334 , GRCh37.p13 chr17: 63,000,013-65,936,105 RPSAP67, HELZ-AS1, 51 more genes
    nsv6994934copy number variation1nstd229human GRCh38 chr17: 68,230,401-68,234,100 , GRCh37.p13 chr17: 66,226,542-66,230,241 , GRCh37.p13 chr17|NW_003871088.1: 290,412-294,111 AMZ2
    nsv6991958copy number variation1nstd229human GRCh38 chr17: 68,236,701-68,245,100 , GRCh37.p13 chr17|NW_003871088.1: 296,712-305,111 , GRCh37.p13 chr17: 66,232,842-66,241,241 AMZ2
    nsv6987609copy number variation1nstd229human GRCh38 chr17: 68,231,415-68,231,636 , GRCh37.p13 chr17: 66,227,556-66,227,777 , GRCh37.p13 chr17|NW_003871088.1: 291,426-291,647 AMZ2
    nsv6987332copy number variation1nstd229human GRCh38 chr17: 68,201,888-68,211,055 , GRCh37.p13 chr17|NW_003871088.1: 261,899-271,066 , GRCh37.p13 chr17: 66,198,029-66,207,196 AMZ2
    nsv6985228copy number variation1nstd229human GRCh38 chr17: 68,253,359-68,259,521 , GRCh37.p13 chr17|NW_003871088.1: 313,370-319,532 , GRCh37.p13 chr17: 66,249,500-66,255,662 ARSG, AMZ2
    nsv6979115copy number variation1nstd229human GRCh38 chr17: 68,216,109-68,220,053 , GRCh37.p13 chr17: 66,212,250-66,216,194 , GRCh37.p13 chr17|NW_003871088.1: 276,120-280,064 AMZ2
    nsv6979114copy number variation1nstd229human GRCh38 chr17: 68,202,618-68,207,183 , GRCh37.p13 chr17: 66,198,759-66,203,324 , GRCh37.p13 chr17|NW_003871088.1: 262,629-267,194 AMZ2
    nsv6637738copy number variation1nstd102humanUncertain significance GRCh37 chr17: 66,075,889-66,268,460 , GRCh38.p12 chr17: 68,079,784-68,272,319 ARSG, ARHGAP27P2, 8 more genes
    nsv6592405inversion1nstd223human GRCh38 chr17: 68,220,858-68,221,537 , GRCh37.p13 chr17|NW_003871088.1: 280,869-281,548 , GRCh37.p13 chr17: 66,216,999-66,217,678 AMZ2
    nsv6588366inversion1nstd223human GRCh38 chr17: 68,216,726-68,218,141 , GRCh37.p13 chr17|NW_003871088.1: 276,737-278,152 , GRCh37.p13 chr17: 66,212,867-66,214,282 AMZ2
    nsv6533126copy number variation1nstd223human GRCh38 chr17: 68,231,415-68,231,636 , GRCh37.p13 chr17: 66,227,556-66,227,777 , GRCh37.p13 chr17|NW_003871088.1: 291,426-291,647 AMZ2
    nsv6527075copy number variation1nstd223human GRCh38 chr17: 68,230,426-68,234,083 , GRCh37.p13 chr17: 66,226,567-66,230,224 , GRCh37.p13 chr17|NW_003871088.1: 290,437-294,094 AMZ2
    nsv6525788copy number variation1nstd223human GRCh38 chr17: 68,202,616-68,207,182 , GRCh37.p13 chr17|NW_003871088.1: 262,627-267,193 , GRCh37.p13 chr17: 66,198,757-66,203,323 AMZ2
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