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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094912copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 63,149,520-63,149,656 , GRCh38.p12 chr17: 65,153,402-65,153,538 RGS9
    nsv7077537inversion1nstd229human GRCh38 chr17: 64,968,697-68,255,761 , GRCh37.p13 chr17: 62,964,815-65,936,105 SNORA38B, PRKCA-AS1, 52 more genes
    nsv7070779inversion1nstd229human GRCh38 chr17: 64,711,213-68,088,947 , GRCh37.p13 chr17: 62,707,331-65,936,105 MICOS10P2, LOC100420638, 61 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
    nsv7059173inversion1nstd229human GRCh38 chr17: 65,003,895-68,220,334 , GRCh37.p13 chr17: 63,000,013-65,936,105 RPSAP67, HELZ-AS1, 51 more genes
    nsv6996191copy number variation1nstd229human GRCh38 chr17: 65,212,196-65,212,360 , GRCh37.p13 chr17: 63,208,314-63,208,478 RGS9
    nsv6995398copy number variation1nstd229human GRCh38 chr17: 65,220,456-65,220,477 , GRCh37.p13 chr17: 63,216,574-63,216,595 RGS9
    nsv6994234copy number variation1nstd229human GRCh38 chr17: 65,219,173-65,222,108 , GRCh37.p13 chr17: 63,215,291-63,218,226 RGS9
    nsv6989900copy number variation1nstd229human GRCh38 chr17: 65,172,606-65,177,140 , GRCh37.p13 chr17: 63,168,724-63,173,258 ZNF848P, RGS9
    nsv6986727copy number variation1nstd229human GRCh38 chr17: 65,178,575-65,181,532 , GRCh37.p13 chr17: 63,174,693-63,177,650 RGS9
    nsv6986067copy number variation1nstd229human GRCh38 chr17: 65,140,886-65,153,412 , GRCh37.p13 chr17: 63,137,004-63,149,530 RGS9
    nsv6979800copy number variation1nstd229human GRCh38 chr17: 65,196,627-65,196,695 , GRCh37.p13 chr17: 63,192,745-63,192,813 RGS9
    nsv6593751inversion1nstd223human GRCh38 chr17: 65,141,964-65,142,612 , GRCh37.p13 chr17: 63,138,082-63,138,730 RGS9
    nsv6592125inversion1nstd223human GRCh38 chr17: 65,161,859-65,162,296 , GRCh37.p13 chr17: 63,157,977-63,158,414 RGS9
    nsv6580898inversion1nstd223human GRCh38 chr17: 65,148,990-65,150,468 , GRCh37.p13 chr17: 63,145,108-63,146,586 RGS9
    nsv6535491copy number variation1nstd223human GRCh38 chr17: 65,142,080-65,146,336 , GRCh37.p13 chr17: 63,138,198-63,142,454 RGS9
    nsv6530149copy number variation1nstd223human GRCh38 chr17: 65,165,140-65,165,462 , GRCh37.p13 chr17: 63,161,258-63,161,580 RGS9
    nsv6522601copy number variation1nstd223human GRCh38 chr17: 65,172,603-65,177,142 , GRCh37.p13 chr17: 63,168,721-63,173,260 ZNF848P, RGS9
    nsv6520843copy number variation1nstd223human GRCh38 chr17: 65,170,333-65,172,333 , GRCh37.p13 chr17: 63,166,451-63,168,451 RGS9
    nsv6310401copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 63,187,690-63,189,718 , GRCh38.p12 chr17: 65,191,572-65,193,600 RGS9
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