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Items: 1 to 20 of 408

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142355copy number variation1nstd232human GRCh37.p13 chr2: 183,866,771-183,866,853 , GRCh38.p12 chr2: 183,002,043-183,002,125 NCKAP1
    nsv7139890insertion1nstd232human GRCh37.p13 chr2: 183,793,628-183,793,628 , GRCh38.p12 chr2: 182,928,900-182,928,900 NCKAP1
    nsv7053910inversion1nstd229human GRCh38 chr2: 182,916,791-182,916,899 , GRCh37.p13 chr2: 183,781,519-183,781,627 NCKAP1
    nsv7051588inversion1nstd229human GRCh38 chr2: 182,952,949-182,953,109 , GRCh37.p13 chr2: 183,817,677-183,817,837 NCKAP1
    nsv6694408copy number variation1nstd229human GRCh38 chr2: 182,991,663-184,070,054 , GRCh37.p13 chr2: 183,856,391-184,934,781 KRT8P10, NCKAP1, 4 more genes
    nsv6691127copy number variation1nstd229human GRCh38 chr2: 182,730,019-183,183,033 , GRCh37.p13 chr2: 183,594,746-184,047,761 DNAJC10, RPL31P15, 6 more genes
    nsv6682586copy number variation1nstd229human GRCh38 chr2: 182,918,501-182,924,400 , GRCh37.p13 chr2: 183,783,229-183,789,128 NCKAP1
    nsv6682133copy number variation1nstd229human GRCh38 chr2: 182,918,601-182,924,300 , GRCh37.p13 chr2: 183,783,329-183,789,028 NCKAP1
    nsv6681643copy number variation1nstd229human GRCh38 chr2: 182,897,501-182,913,200 , GRCh37.p13 chr2: 183,762,229-183,777,928 NCKAP1
    nsv6636434copy number variation1nstd102humanUncertain significance GRCh37 chr2: 183,206,179-184,174,590 , GRCh38.p12 chr2: 182,341,452-183,309,862 DNAJC10, LIN28AP1, 9 more genes
    nsv6636283copy number variation1nstd102humanUncertain significance GRCh37 chr2: 183,070,475-186,717,885 , GRCh38.p12 chr2: 182,205,748-185,853,158 LOC101929976, LOC105373781, 28 more genes
    nsv6551432inversion1nstd223human GRCh38 chr2: 182,922,861-182,923,464 , GRCh37.p13 chr2: 183,787,589-183,788,192 NCKAP1
    nsv6548079inversion1nstd223human GRCh38 chr2: 178,157,654-187,669,944 , GRCh37.p13 chr2: 179,022,381-188,534,671 RNU7-104P, RN7SKP42, 90 more genes
    nsv6352654copy number variation1nstd223human GRCh38 chr2: 182,980,101-182,980,700 , GRCh37.p13 chr2: 183,844,829-183,845,428 NCKAP1
    nsv6352340copy number variation1nstd223human GRCh38 chr2: 183,031,436-183,032,041 , GRCh37.p13 chr2: 183,896,164-183,896,769 NCKAP1
    nsv6348156copy number variation1nstd223human GRCh38 chr2: 182,926,159-182,926,871 , GRCh37.p13 chr2: 183,790,887-183,791,599 NCKAP1
    nsv6346673copy number variation1nstd223human GRCh38 chr2: 182,912,721-182,913,497 , GRCh37.p13 chr2: 183,777,449-183,778,225 NCKAP1
    nsv6338874copy number variation1nstd223human GRCh38 chr2: 182,924,801-182,926,100 , GRCh37.p13 chr2: 183,789,529-183,790,828 NCKAP1
    nsv6338349copy number variation1nstd223human GRCh38 chr2: 182,926,801-182,927,500 , GRCh37.p13 chr2: 183,791,529-183,792,228 NCKAP1
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
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