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Items: 1 to 20 of 586

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137193copy number variation1nstd102humanPathogenic GRCh38 chr17: 68,364,558-68,373,426 , GRCh37 chr17: 66,360,699-66,369,567 ARSG
    nsv7095412copy number variation1nstd102humanUncertain significance GRCh37 chr17: 66,364,669-66,364,905 , GRCh38.p12 chr17: 68,368,528-68,368,764 ARSG
    nsv7095360copy number variation1nstd102humanUncertain significance GRCh37 chr17: 66,352,788-66,352,965 , GRCh38.p12 chr17: 68,356,647-68,356,824 ARSG
    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
    nsv7058983inversion1nstd229human GRCh38 chr17: 68,258,315-68,258,447 , GRCh37.p13 chr17|NW_003871088.1: 318,326-318,458 , GRCh37.p13 chr17: 66,254,456-66,254,588 ARSG
    nsv6996511copy number variation1nstd229human GRCh38 chr17: 68,385,915-68,398,237 , GRCh37.p13 chr17: 66,382,056-66,394,378 ARSG, TRUND-NNN5-1
    nsv6995681copy number variation1nstd229human GRCh38 chr17: 68,306,979-68,311,955 , GRCh37.p13 chr17|NW_003871088.1: 366,990-371,966 , GRCh37.p13 chr17: 66,303,120-66,308,096 ARSG
    nsv6994519copy number variation1nstd229human GRCh38 chr17: 68,314,205-68,317,476 , GRCh37.p13 chr17: 66,310,346-66,313,617 , GRCh37.p13 chr17|NW_003871088.1: 374,216-377,487 ARSG
    nsv6994082copy number variation1nstd229human GRCh38 chr17: 68,374,748-68,391,606 , GRCh37.p13 chr17: 66,370,889-66,387,747 ARSG
    nsv6990602copy number variation1nstd229human GRCh38 chr17: 68,351,210-68,353,267 , GRCh37.p13 chr17: 66,347,351-66,349,408 ARSG
    nsv6987927copy number variation1nstd229human GRCh38 chr17: 68,384,864-68,389,235 , GRCh37.p13 chr17: 66,381,005-66,385,376 ARSG
    nsv6987914copy number variation1nstd229human GRCh38 chr17: 68,450,620-68,450,806 , GRCh37.p13 chr17: 66,446,761-66,446,947 ARSG, PRKAR1A, 1 more genes
    nsv6986720copy number variation1nstd229human GRCh38 chr17: 68,437,588-68,437,947 , GRCh37.p13 chr17: 66,433,729-66,434,088 PRKAR1A, WIPI1, 1 more genes
    nsv6986516copy number variation1nstd229human GRCh38 chr17: 68,315,952-68,319,451 , GRCh37.p13 chr17|NW_003871088.1: 375,963-379,462 , GRCh37.p13 chr17: 66,312,093-66,315,592 ARSG
    nsv6986147copy number variation1nstd229human GRCh38 chr17: 68,428,365-68,428,621 , GRCh37.p13 chr17: 66,424,506-66,424,762 ARSG, PRKAR1A, 1 more genes
    nsv6985926copy number variation1nstd229human GRCh38 chr17: 68,275,989-68,276,024 , GRCh37.p13 chr17|NW_003871088.1: 336,000-336,035 , GRCh37.p13 chr17: 66,272,130-66,272,165 ARSG, SLC16A6
    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
    nsv6985181copy number variation1nstd229human GRCh38 chr17: 68,356,371-68,360,522 , GRCh37.p13 chr17: 66,352,512-66,356,663 ARSG
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