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Items: 1 to 20 of 369

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7050777inversion1nstd229human GRCh38 chr2: 117,420,323-122,585,255 , GRCh37.p13 chr2: 118,177,899-123,342,831 LOC105373578, RPL17P15, 65 more genes
    nsv7044064inversion1nstd229human GRCh38 chr2: 112,019,946-120,004,832 , GRCh37.p13 chr2: 112,777,523-120,762,408 LOC105373563, IL1A, 112 more genes
    nsv6697338copy number variation1nstd229human GRCh38 chr2: 119,485,999-119,492,765 , GRCh37.p13 chr2: 120,243,575-120,250,341 SCTR-AS1, SCTR
    nsv6696024copy number variation1nstd229human GRCh38 chr2: 119,502,218-119,502,259 , GRCh37.p13 chr2: 120,259,794-120,259,835 SCTR
    nsv6695409copy number variation1nstd229human GRCh38 chr2: 119,512,435-119,512,494 , GRCh37.p13 chr2: 120,270,011-120,270,070 SCTR
    nsv6691400copy number variation1nstd229human GRCh38 chr2: 119,484,568-119,487,635 , GRCh37.p13 chr2: 120,242,144-120,245,211 SCTR, SCTR-AS1
    nsv6689257copy number variation1nstd229human GRCh38 chr2: 119,463,922-119,468,569 , GRCh37.p13 chr2: 120,221,498-120,226,145 SCTR
    nsv6685761copy number variation1nstd229human GRCh38 chr2: 119,391,683-119,531,219 , GRCh37.p13 chr2: 120,149,259-120,288,795 SCTR, SCTR-AS1, 1 more genes
    nsv6685036copy number variation1nstd229human GRCh38 chr2: 119,444,002-119,457,569 , GRCh37.p13 chr2: 120,201,578-120,215,145 SCTR
    nsv6684750copy number variation1nstd229human GRCh38 chr2: 119,452,819-119,467,128 , GRCh37.p13 chr2: 120,210,395-120,224,704 SCTR
    nsv6684059copy number variation1nstd229human GRCh38 chr2: 119,491,532-119,492,081 , GRCh37.p13 chr2: 120,249,108-120,249,657 SCTR
    nsv6680876copy number variation1nstd229human GRCh38 chr2: 119,454,698-119,461,731 , GRCh37.p13 chr2: 120,212,274-120,219,307 SCTR
    nsv6680701copy number variation1nstd229human GRCh38 chr2: 119,439,326-119,443,097 , GRCh37.p13 chr2: 120,196,902-120,200,673 SCTR
    nsv6679459copy number variation1nstd229human GRCh38 chr2: 119,311,516-119,861,317 , GRCh37.p13 chr2: 120,069,092-120,618,893 RPL17P15, TMEM177, 8 more genes
    nsv6636976copy number variation1nstd102humanUncertain significance GRCh37 chr2: 120,079,538-120,626,557 , GRCh38.p12 chr2: 119,321,962-119,868,981 TMEM177, RPL17P15, 8 more genes
    nsv6636871copy number variation1nstd102humanPathogenic GRCh37 chr2: 116,761,476-123,897,262 , GRCh38.p12 chr2: 116,003,900-123,139,686 LOC105373578, RPL17P15, 78 more genes
    nsv6553311inversion1nstd223human GRCh38 chr2: 113,382,126-121,687,299 , GRCh37.p13 chr2: 114,139,703-122,444,875 RPSAP23, CCDC93, 98 more genes
    nsv6552404inversion1nstd223human GRCh38 chr2: 119,516,688-119,517,450 , GRCh37.p13 chr2: 120,274,264-120,275,026 SCTR
    nsv6349537copy number variation1nstd223human GRCh38 chr2: 119,247,614-119,525,129 , GRCh37.p13 chr2: 120,005,190-120,282,705 SCTR, C2orf76, 6 more genes
    nsv6345854copy number variation1nstd223human GRCh38 chr2: 119,497,301-119,499,700 , GRCh37.p13 chr2: 120,254,877-120,257,276 SCTR
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