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Items: 1 to 20 of 450

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137216copy number variation1nstd102humanPathogenic GRCh37 chr17: 30,572,862-35,843,988 , GRCh38.p12 chr17: 32,245,843-36,446,544 PSMD11, C17orf50, 117 more genes
    nsv7098907copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,138,501-37,924,067 , GRCh37.p13 chr17: 34,900,240-35,888,667 LOC102723414, SYNRG, 51 more genes
    nsv7073998inversion1nstd229human GRCh38 chr17: 32,918,710-41,148,753 , GRCh37.p13 chr17: 31,245,728-39,305,005 LOC105371750, C17orf78, 298 more genes
    nsv6637369copy number variation1nstd102humanPathogenic GRCh37 chr17: 34,425,363-36,404,555 , GRCh38.p12 chr17|NT_187614.1: 332,891-2,283,620 CCL3L3, MRM1, 63 more genes
    nsv6624271copy number variation1nstd224human GRCh37 chr17: 34,391,721-34,819,750 , GRCh38.p12 chr17|NT_187614.1: 299,249-698,812 LOC101060212, LOC101927369, 20 more genes
    nsv6513850copy number variation1nstd223human GRCh38 chr17: 36,351,001-36,630,200 , GRCh37.p13 chr17|NW_003315949.1: 235,757-429,138 MYO19, DHRS11, 14 more genes
    nsv6499640copy number variation1nstd223human GRCh37.p13 chr17|NW_003315949.1: 317,653-413,148 , GRCh38 chr17: 36,432,901-36,528,400 LOC105371749, MYO19, 4 more genes
    nsv6495692copy number variation1nstd223human GRCh38 chr17: 36,168,964-36,453,032 , GRCh37.p13 chr17|NW_003315949.1: 53,702-337,782 , TBC1D3I, 13 more genes
    nsv6315528copy number variation1nstd102humanPathogenic GRCh37 chr17: 34,463,923-36,410,559 , GRCh38.p12 chr17|NT_187614.1: 371,451-2,289,624 LOC105371750, DDX52, 60 more genes
    nsv6146096copy number variation1nstd206human GRCh38 chr17: 36,421,980-36,441,990 , GRCh37.p13 chr17|NW_003315949.1: 306,732-326,742 TBC1D3F, LOC100420852
    nsv6145850copy number variation1nstd206human GRCh38 chr17: 36,095,490-38,260,000 , GRCh37.p13 chr17: 34,422,828-36,416,003 , PIGW, 70 more genes
    nsv6133307copy number variation1nstd213human GRCh37 chr17: 34,740,000-36,710,001 , GRCh38.p12 chr17: 36,371,412-38,545,803 , GRCh38.p12 chr17|NT_187614.1: 694,163-2,589,067 TADA2A, SYNRG, 64 more genes
    nsv5932561copy number variation1nstd209human GRCh38 chr17: 36,271,341-37,995,711 , GRCh37.p13 chr17: 34,900,240-35,888,667 LOC101060212, RNU6-1192P, 47 more genes
    nsv5584741copy number variation1nstd207human GRCh38 chr17: 36,175,811-36,438,741 , GRCh37.p13 chr17|NW_003315949.1: 60,551-323,493 , TBC1D3I, 12 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5517916copy number variation1nstd206human GRCh37.p13 chr17|NW_003315949.1: 320,732-429,138 , GRCh38 chr17: 36,435,980-36,562,000 ZNHIT3, GGNBP2, 6 more genes
    nsv5426860copy number variation1nstd206human GRCh38 chr17: 36,168,759-36,452,839 , GRCh37.p13 chr17|NW_003315949.1: 53,497-337,589 , CCL3L3, 13 more genes
    nsv5300334copy number variation1nstd204human GRCh38.p13 chr17: 36,392,201-36,435,800 , GRCh37.p13 chr17|NW_003315949.1: 276,951-320,552 LOC100420852, RNU6-1192P, 1 more genes
    nsv5296272copy number variation1nstd204human GRCh38.p13 chr17: 36,432,101-36,432,700 , GRCh37.p13 chr17|NW_003315949.1: 316,853-317,452 TBC1D3F
    nsv5295020copy number variation1nstd204human GRCh38.p13 chr17: 36,435,801-36,442,900 , GRCh37.p13 chr17|NW_003315949.1: 320,553-327,650 TBC1D3F
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