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Items: 1 to 20 of 114

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv6897521copy number variation1nstd229human GRCh38 chr10: 116,595,727-116,900,521 , GRCh37.p13 chr10: 118,355,239-118,544,777 , GRCh37.p13 chr10|NW_003871069.1: 6,723-196,262 HSPA12A, MIR9851, 8 more genes
    nsv6893705copy number variation1nstd229human GRCh38 chr10: 116,770,590-116,773,422 , GRCh37.p13 chr10: 118,530,101-118,532,933 , GRCh37.p13 chr10|NW_003871069.1: 181,586-184,418 HSPA12A, LOC105378498
    nsv6892782copy number variation1nstd229human GRCh38 chr10: 116,410,808-116,781,748 , GRCh37.p13 chr10|NW_003871069.1: 1-192,744 , GRCh37.p13 chr10: 118,348,517-118,541,259 HSPA12A-AS1, RPL5P27, 10 more genes
    nsv6881779copy number variation1nstd229human GRCh38 chr10: 116,767,379-116,799,629 , GRCh37.p13 chr10: 118,526,890-118,544,777 , GRCh37.p13 chr10|NW_003871069.1: 178,375-196,262 HSPA12A, LOC105378498
    nsv6314129copy number variation1nstd102humanPathogenic GRCh37 chr10: 117,019,650-125,217,066 , GRCh38.p12 chr10: 115,260,173-123,457,550 PDZD8, MIR3663HG, 122 more genes
    nsv6314085copy number variation1nstd102humanPathogenic GRCh37 chr10: 108,455,687-135,427,143 , GRCh38.p12 chr10: 106,695,929-133,613,639 LOC107984268, DPYSL4, 379 more genes
    nsv6184328copy number variation1nstd214human GRCh38 chr10: 116,770,945-116,770,999 , GRCh37.p13 chr10|NW_003871069.1: 181,941-181,995 , GRCh37.p13 chr10: 118,530,456-118,530,510 LOC105378498, HSPA12A
    nsv6131932copy number variation1nstd213human GRCh37 chr10: 115,960,000-125,870,001 , GRCh38.p12 chr10: 114,200,241-124,109,956 ACADSB, DMBT1, 148 more genes
    nsv6131852copy number variation1nstd213human GRCh37 chr10: 118,380,000-118,640,001 , GRCh38.p12 chr10: 116,620,488-116,880,490 PNLIPRP2, SHTN1, 7 more genes
    nsv6131766copy number variation1nstd213human GRCh37 chr10: 116,010,000-125,870,001 , GRCh38.p12 chr10: 114,250,241-124,109,956 ACADSB, DMBT1, 146 more genes
    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
    nsv5974801inversion1nstd209human GRCh38 chr10: 116,446,135-119,236,441 , GRCh37.p13 chr10: 118,205,647-120,995,953 EMX2, PRLHR, 48 more genes
    nsv5925970copy number variation1nstd209human GRCh38 chr10: 116,770,945-116,770,999 , GRCh37.p13 chr10|NW_003871069.1: 181,941-181,995 , GRCh37.p13 chr10: 118,530,456-118,530,510 HSPA12A, LOC105378498
    nsv5539341insertion1nstd206human GRCh38 chr10: 116,770,890-116,770,940 , GRCh37.p13 chr10: 118,530,401-118,530,451 , GRCh37.p13 chr10|NW_003871069.1: 181,886-181,936 HSPA12A, LOC105378498
    nsv4977105copy number variation1nstd200human GRCh38 chr10: 116,770,590-116,773,416 , GRCh37.p13 chr10: 118,530,101-118,532,927 , GRCh37.p13 chr10|NW_003871069.1: 181,586-184,412 LOC105378498, HSPA12A
    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
    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
    nsv4832445copy number variation1nstd200human GRCh37 chr10: 118,519,005-118,535,588 , GRCh38.p12 chr10: 116,759,494-116,776,077 HSPA12A, LOC105378498
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