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Items: 1 to 20 of 324

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057623inversion1nstd229human GRCh38 chr2: 240,589,655-240,589,864 , GRCh37.p13 chr2: 241,529,072-241,529,281 CAPN10
    nsv7054682inversion1nstd229human GRCh38 chr2: 240,561,802-240,635,377 , GRCh37.p13 chr2: 241,501,219-241,574,794 RNPEPL1, DUSP28, 3 more genes
    nsv6710725copy number variation1nstd229human GRCh38 chr2: 240,108,601-241,272,500 , GRCh37.p13 chr2: 241,048,018-242,211,915 LOC112268440, CAPN10-DT, 34 more genes
    nsv6708981copy number variation1nstd229human GRCh38 chr2: 240,521,589-240,586,617 , GRCh37.p13 chr2: 241,461,006-241,526,034 CAPN10, RNPEPL1, 3 more genes
    nsv6700895copy number variation1nstd229human GRCh38 chr2: 240,585,461-240,591,134 , GRCh37.p13 chr2: 241,524,878-241,530,551 CAPN10-DT, CAPN10
    nsv6699925copy number variation1nstd229human GRCh38 chr2: 240,479,729-240,606,103 , GRCh37.p13 chr2: 241,419,146-241,545,520 CAPN10-DT, GPR35, 4 more genes
    nsv6636841copy number variation1nstd102humanPathogenic GRCh37 chr2: 236,878,509-242,783,384 , GRCh38.p12 chr2: 235,969,865-241,841,232 COPS8-DT, MTND5P46, 128 more genes
    nsv6636797copy number variation1nstd102humanUncertain significance GRCh37 chr2: 241,402,844-241,572,457 , GRCh38.p12 chr2: 240,463,427-240,633,040 GPR35, RNPEPL1, 5 more genes
    nsv6636673copy number variation1nstd102humanPathogenic GRCh37 chr2: 235,942,616-242,783,384 , GRCh38.p12 chr2: 235,033,972-241,841,232 LINC02991, OR6B3, 136 more genes
    nsv6634398copy number variation1nstd102humanPathogenic GRCh37 chr2: 239,229,304-243,199,373 , GRCh38.p12 chr2: 238,320,663-242,157,305 HDAC4-AS1, ING5, 92 more genes
    nsv6628080copy number variation1nstd224human GRCh37 chr2: 241,536,126-241,570,284 , GRCh38.p12 chr2: 240,596,709-240,630,867 GPR35, CAPN10
    nsv6628022copy number variation1nstd224human GRCh37 chr2: 241,537,306-241,579,108 , GRCh38.p12 chr2: 240,597,889-240,639,691 CAPN10, GPR35
    nsv6627576copy number variation1nstd224human GRCh37 chr2: 241,538,074-241,579,108 , GRCh38.p12 chr2: 240,598,657-240,639,691 CAPN10, GPR35
    nsv6348430copy number variation1nstd223human GRCh38 chr2: 237,953,314-241,782,040 , GRCh37.p13 chr2: 238,861,956-242,721,455 HDLBP-AS1, TWIST2, 90 more genes
    nsv6344873copy number variation1nstd223human GRCh38 chr2: 240,582,795-240,647,753 , GRCh37.p13 chr2: 241,522,212-241,587,170 CAPN10, GPR35, 1 more genes
    nsv6341490copy number variation1nstd223human GRCh38 chr2: 240,584,243-240,586,554 , GRCh37.p13 chr2: 241,523,660-241,525,971 CAPN10, CAPN10-DT
    nsv6315457copy number variation1nstd102humanPathogenic GRCh37 chr2: 236,472,789-242,783,384 , GRCh38.p12 chr2: 235,564,145-241,841,232 AGAP1, OR5S1P, 130 more genes
    nsv6315436copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,227,837-242,783,384 , GRCh38.p12 chr2: 232,363,127-241,841,232 LOC105373929, LOC105373932, 204 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314846copy number variation1nstd102humanPathogenic GRCh38 chr2: 236,710,422-242,106,504 , GRCh37.p13 chr2: 237,619,065-243,048,655 LINC01937, FAM240C, 126 more genes
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