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Items: 1 to 20 of 167

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv5980211insertion1nstd209human GRCh38 chr10: 116,633,652-116,633,652 , GRCh37.p13 chr10: 118,393,163-118,393,163 , GRCh37.p13 chr10|NW_003871069.1: 44,648-44,648 PNLIPRP2
    nsv5974801inversion1nstd209human GRCh38 chr10: 116,446,135-119,236,441 , GRCh37.p13 chr10: 118,205,647-120,995,953 EMX2, PRLHR, 48 more genes
    nsv5916633copy number variation1nstd209human GRCh38 chr10: 116,636,468-116,636,543 , GRCh37.p13 chr10|NW_003871069.1: 47,464-47,539 , GRCh37.p13 chr10: 118,395,979-118,396,054 PNLIPRP2
    nsv5643412insertion1nstd207human GRCh38 chr10: 116,633,652-116,633,652 , GRCh37.p13 chr10: 118,393,163-118,393,163 , GRCh37.p13 chr10|NW_003871069.1: 44,648-44,648 PNLIPRP2
    nsv5640003insertion1nstd207human GRCh38 chr10: 116,633,922-116,633,922 , GRCh37.p13 chr10: 118,393,433-118,393,433 , GRCh37.p13 chr10|NW_003871069.1: 44,918-44,918 PNLIPRP2
    nsv5631438insertion1nstd207human GRCh38 chr10: 116,634,007-116,634,007 , GRCh37.p13 chr10|NW_003871069.1: 45,003-45,003 , GRCh37.p13 chr10: 118,393,518-118,393,518 PNLIPRP2
    nsv5627606insertion1nstd207human GRCh38 chr10: 116,633,670-116,633,670 , GRCh37.p13 chr10|NW_003871069.1: 44,666-44,666 , GRCh37.p13 chr10: 118,393,181-118,393,181 PNLIPRP2
    nsv5604258copy number variation1nstd207human GRCh38 chr10: 116,633,719-116,633,784 , GRCh37.p13 chr10|NW_003871069.1: 44,715-44,780 , GRCh37.p13 chr10: 118,393,230-118,393,295 PNLIPRP2
    nsv5508963copy number variation1nstd206human GRCh38 chr10: 116,636,811-116,638,159 , GRCh37.p13 chr10|NW_003871069.1: 47,807-49,155 , GRCh37.p13 chr10: 118,396,322-118,397,670 PNLIPRP2
    nsv5507533copy number variation1nstd206human GRCh38 chr10: 116,634,283-116,634,410 , GRCh37.p13 chr10|NW_003871069.1: 45,279-45,406 , GRCh37.p13 chr10: 118,393,794-118,393,921 PNLIPRP2
    nsv4977099copy number variation1nstd200human GRCh38 chr10: 116,632,730-116,636,629 , GRCh37.p13 chr10|NW_003871069.1: 43,726-47,625 , GRCh37.p13 chr10: 118,392,241-118,396,140 PNLIPRP2
    nsv4974084copy number variation1nstd200human GRCh38 chr10: 116,595,727-116,900,521 , GRCh37.p13 chr10|NW_003871069.1: 6,723-196,262 , GRCh37.p13 chr10: 118,355,239-118,544,777 HSPA12A, SPMIP5, 8 more genes
    nsv4845500copy number variation1nstd200human GRCh37 chr10: 118,393,794-118,393,921 , GRCh38.p12 chr10: 116,634,283-116,634,410 PNLIPRP2
    nsv4844089copy number variation1nstd200human GRCh37 chr10: 118,392,241-118,396,140 , GRCh38.p12 chr10: 116,632,730-116,636,629 PNLIPRP2
    nsv4841657copy number variation1nstd200human GRCh37 chr10: 118,355,239-118,660,032 , GRCh38.p12 chr10: 116,595,727-116,900,521 HSPA12A-AS1, PNLIPRP2, 8 more genes
    nsv4764489insertion1nstd199human GRCh37 chr10: 118,393,158-118,393,158 , GRCh38.p12 chr10: 116,633,647-116,633,647 PNLIPRP2
    nsv4701805copy number variation1nstd195human GRCh37 chr10: 118,387,897-118,387,898 , GRCh38.p12 chr10: 116,628,386-116,628,387 PNLIPRP2
    nsv4574702mobile element insertion1nstd166human GRCh37.p13 chr10: 118,404,606-118,404,606 , GRCh38.p12 chr10: 116,645,095-116,645,095 PNLIPRP2
    nsv4528147copy number variation1nstd166human GRCh37.p13 chr10: 118,359,852-118,569,817 , GRCh38.p12 chr10: 116,600,340-116,810,306 PNLIPRP1, PNLIPRP2, 5 more genes
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