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Items: 1 to 20 of 318

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096928copy number variation1nstd102humanUncertain significance GRCh37 chr3: 123,003,455-125,313,644 , GRCh38.p12 chr3: 123,284,608-125,594,800 MIR544B, OSBPL11, 33 more genes
    nsv7096531copy number variation1nstd102humanUncertain significance GRCh37 chr3: 121,489,192-125,313,644 , GRCh38.p12 chr3: 121,770,345-125,594,800 MEMO1P6, HACD2, 62 more genes
    nsv7039961inversion1nstd229human GRCh38 chr3: 125,220,024-129,368,164 , GRCh37.p13 chr3: 124,938,868-129,087,007 MARK3P3, RAB43, 120 more genes
    nsv6716873copy number variation1nstd229human GRCh38 chr3: 125,512,032-125,517,144 , GRCh37.p13 chr3: 125,230,876-125,235,988 SNX4
    nsv6713848copy number variation1nstd229human GRCh38 chr3: 125,379,501-125,511,300 , GRCh37.p13 chr3: 125,098,345-125,230,144 LOC105374081, RNU6-232P, 2 more genes
    nsv6713394copy number variation1nstd229human GRCh38 chr3: 125,439,790-125,446,499 , GRCh37.p13 chr3: 125,158,634-125,165,343 SNX4
    nsv6710779copy number variation1nstd229human GRCh38 chr3: 125,082,194-128,829,123 , GRCh37.p13 chr3: 124,801,038-128,547,966 LOC105374094, DNAJB8-AS1, 98 more genes
    nsv6703931copy number variation1nstd229human GRCh38 chr3: 118,573,267-126,079,281 , GRCh37.p13 chr3: 118,292,114-125,798,124 RPS24P9, LOC105374064, 149 more genes
    nsv6701167copy number variation1nstd229human GRCh38 chr3: 125,379,401-125,479,800 , GRCh37.p13 chr3: 125,098,245-125,198,644 LOC105374081, RNU6-232P, 2 more genes
    nsv6700932copy number variation1nstd229human GRCh38 chr3: 125,458,855-125,458,885 , GRCh37.p13 chr3: 125,177,699-125,177,729 SNX4
    nsv6698859copy number variation1nstd229human GRCh38 chr3: 125,469,705-125,474,247 , GRCh37.p13 chr3: 125,188,549-125,193,091 SNX4
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6571472inversion1nstd223human GRCh38 chr3: 125,457,827-125,458,466 , GRCh37.p13 chr3: 125,176,671-125,177,310 SNX4
    nsv6570481inversion1nstd223human GRCh38 chr3: 125,465,267-125,466,808 , GRCh37.p13 chr3: 125,184,111-125,185,652 SNX4
    nsv6567951inversion1nstd223human GRCh38 chr3: 125,475,507-125,476,060 , GRCh37.p13 chr3: 125,194,351-125,194,904 SNX4
    nsv6566210inversion1nstd223human GRCh38 chr3: 125,448,990-125,449,361 , GRCh37.p13 chr3: 125,167,834-125,168,205 SNX4
    nsv6565724inversion1nstd223human GRCh38 chr3: 125,457,589-125,458,820 , GRCh37.p13 chr3: 125,176,433-125,177,664 SNX4
    nsv6564935inversion1nstd223human GRCh38 chr3: 125,484,399-125,484,988 , GRCh37.p13 chr3: 125,203,243-125,203,832 SNX4
    nsv6563759inversion1nstd223human GRCh38 chr3: 125,500,292-125,500,414 , GRCh37.p13 chr3: 125,219,136-125,219,258 SNX4
    nsv6562994inversion1nstd223human GRCh38 chr3: 125,457,594-125,459,144 , GRCh37.p13 chr3: 125,176,438-125,177,988 SNX4
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