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Items: 1 to 20 of 289

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7136970copy number variation1nstd102humanUncertain significance GRCh38 chr2: 128,262,169-128,275,055 , GRCh37.p13 chr2: 129,019,743-129,032,629 HS6ST1
    nsv7096197copy number variation1nstd102humanPathogenic GRCh37 chr2: 127,806,102-129,076,137 , GRCh38.p12 chr2: 127,048,526-128,318,563 IWS1, ZFP91P1, 35 more genes
    nsv7095855copy number variation1nstd102humanUncertain significance GRCh37 chr2: 129,025,736-129,026,464 , GRCh38.p12 chr2: 128,268,162-128,268,890 HS6ST1
    nsv7095853copy number variation1nstd102humanPathogenic GRCh37 chr2: 127,451,420-129,076,137 , GRCh38.p12 chr2: 126,693,844-128,318,563 SRMP3, DYNLT3P2, 41 more genes
    nsv7052248inversion1nstd229human GRCh38 chr2: 128,261,338-128,280,102 , GRCh37.p13 chr2: 129,018,912-129,037,676 HS6ST1
    nsv7051453inversion1nstd229human GRCh38 chr2: 127,202,996-128,332,828 , GRCh37.p13 chr2: 127,960,572-129,090,402 WDR33, RNU4-48P, 32 more genes
    nsv6697221copy number variation1nstd229human GRCh38 chr2: 128,288,736-128,288,790 , GRCh37.p13 chr2: 129,046,310-129,046,364 HS6ST1
    nsv6695964copy number variation1nstd229human GRCh38 chr2: 128,262,860-128,274,185 , GRCh37.p13 chr2: 129,020,434-129,031,759 HS6ST1
    nsv6694450copy number variation1nstd229human GRCh38 chr2: 128,251,947-128,531,875 , GRCh37.p13 chr2: 129,009,521-129,289,449 LOC105373610, RNA5SP103, 3 more genes
    nsv6694316copy number variation1nstd229human GRCh38 chr2: 128,097,810-128,417,306 , GRCh37.p13 chr2: 128,855,384-129,174,880 SRMP3, LOC105373610, 6 more genes
    nsv6690568copy number variation1nstd229human GRCh38 chr2: 128,279,604-128,280,240 , GRCh37.p13 chr2: 129,037,178-129,037,814 HS6ST1
    nsv6688828copy number variation1nstd229human GRCh38 chr2: 127,436,502-128,393,799 , GRCh37.p13 chr2: 128,194,078-129,151,373 LOC107985944, LOC105373610, 25 more genes
    nsv6688269copy number variation1nstd229human GRCh38 chr2: 128,314,385-128,314,771 , GRCh37.p13 chr2: 129,071,959-129,072,345 HS6ST1
    nsv6688020copy number variation1nstd229human GRCh38 chr2: 128,291,133-128,299,109 , GRCh37.p13 chr2: 129,048,707-129,056,683 HS6ST1
    nsv6684988copy number variation1nstd229human GRCh38 chr2: 128,281,990-128,302,560 , GRCh37.p13 chr2: 129,039,564-129,060,134 HS6ST1
    nsv6684987copy number variation1nstd229human GRCh38 chr2: 128,298,220-128,298,317 , GRCh37.p13 chr2: 129,055,794-129,055,891 HS6ST1
    nsv6684837copy number variation1nstd229human GRCh38 chr2: 128,302,900-128,307,466 , GRCh37.p13 chr2: 129,060,474-129,065,040 HS6ST1
    nsv6680793copy number variation1nstd229human GRCh38 chr2: 128,284,650-128,292,688 , GRCh37.p13 chr2: 129,042,224-129,050,262 HS6ST1
    nsv6680085copy number variation1nstd229human GRCh38 chr2: 128,307,230-128,313,143 , GRCh37.p13 chr2: 129,064,804-129,070,717 HS6ST1
    nsv6353670copy number variation1nstd223human GRCh38 chr2: 128,262,860-128,274,185 , GRCh37.p13 chr2: 129,020,434-129,031,759 HS6ST1
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