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Items: 1 to 20 of 195

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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
    nsv5980446copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718 LINC02641, CFAP46, 194 more genes
    nsv5925648copy number variation1nstd209human GRCh38 chr10: 122,480,198-122,483,352 , GRCh37.p13 chr10: 124,239,714-124,242,868 HTRA1
    nsv5865901copy number variation1nstd209human GRCh38 chr10: 122,480,150-122,483,386 , GRCh37.p13 chr10: 124,239,666-124,242,902 HTRA1
    nsv5672603copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 119,302,758-124,813,305 , GRCh38.p12 chr10: 117,543,247-123,053,789 ACADSB, DMBT1, 84 more genes
    nsv5644499insertion1nstd207human GRCh38 chr10: 122,507,958-122,507,958 , GRCh37.p13 chr10: 124,267,474-124,267,474 HTRA1
    nsv5509867copy number variation1nstd206human GRCh38 chr10: 122,469,014-122,469,767 , GRCh37.p13 chr10: 124,228,530-124,229,283 HTRA1
    nsv5504605copy number variation1nstd206human GRCh38 chr10: 122,503,265-122,504,236 , GRCh37.p13 chr10: 124,262,781-124,263,752 HTRA1
    nsv5496957copy number variation1nstd206human GRCh38 chr10: 122,480,201-122,483,353 , GRCh37.p13 chr10: 124,239,717-124,242,869 HTRA1
    nsv5354535translocation1nstd200human GRCh38 chr10: 122,480,201-122,480,201 , GRCh38 chr10: 122,483,353-122,483,353 , GRCh37.p13 chr10: 124,242,869-124,242,869 , GRCh37.p13 chr10: 124,239,717-124,239,717 HTRA1
    nsv5342041translocation1nstd200human GRCh37 chr10: 124,239,717-124,239,717 , GRCh37 chr10: 124,242,869-124,242,869 , GRCh38.p12 chr10: 122,483,353-122,483,353 , GRCh38.p12 chr10: 122,480,201-122,480,201 HTRA1
    nsv5336837translocation1nstd200human GRCh37 chr10: 124,258,513-124,258,513 , GRCh37 chr10: 124,259,634-124,259,634 , GRCh38.p12 chr10: 122,498,997-122,498,997 , GRCh38.p12 chr10: 122,500,118-122,500,118 HTRA1
    nsv5301357copy number variation1nstd204human GRCh38.p13 chr10: 122,480,177-122,483,382 , GRCh37.p13 chr10: 124,239,693-124,242,898 HTRA1
    nsv5247811copy number variation1nstd204human GRCh38.p13 chr10: 122,480,200-122,483,286 , GRCh37.p13 chr10: 124,239,716-124,242,802 HTRA1
    nsv5240759copy number variation1nstd204human GRCh38.p13 chr10: 122,479,701-122,483,200 , GRCh37.p13 chr10: 124,239,217-124,242,716 HTRA1
    nsv5136974mobile element insertion1nstd203human GRCh38 chr10: 122,496,228-122,496,259 , GRCh37.p13 chr10: 124,255,744-124,255,775 , HTRA1
    nsv5125576mobile element insertion1nstd203human GRCh38 chr10: 122,478,392-122,478,410 , GRCh37.p13 chr10: 124,237,908-124,237,926 HTRA1
    nsv4983951copy number variation1nstd200human GRCh38 chr10: 122,478,215-122,566,021 , GRCh37.p13 chr10: 124,237,731-124,325,537 , DMBT1, 1 more genes
    nsv4977307copy number variation1nstd200human GRCh38 chr10: 122,477,117-122,478,527 , GRCh37.p13 chr10: 124,236,633-124,238,043 HTRA1
    nsv4977306copy number variation1nstd200human GRCh38 chr10: 122,469,875-122,477,340 , GRCh37.p13 chr10: 124,229,391-124,236,856 HTRA1
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