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Items: 1 to 20 of 201

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098872copy number variation1nstd102humanUncertain significance GRCh37 chr2: 73,716,761-75,347,894 , GRCh38.p12 chr2: 73,489,634-75,120,768 RTKN, PCGF1, 61 more genes
    nsv7053626inversion1nstd229human GRCh38 chr2: 74,662,166-74,668,822 , GRCh37.p13 chr2: 74,889,293-74,895,949 SEMA4F
    nsv7039989inversion1nstd229human GRCh38 chr2: 74,303,206-79,264,856 , GRCh37.p13 chr2: 74,530,333-79,491,982 WBP1, DCTN1-AS1, 80 more genes
    nsv6697570copy number variation1nstd229human GRCh38 chr2: 74,645,014-74,781,337 , GRCh37.p13 chr2: 74,872,141-75,008,464 M1AP, SEMA4F, 3 more genes
    nsv6694019copy number variation1nstd229human GRCh38 chr2: 74,664,721-75,043,601 , GRCh37.p13 chr2: 74,891,848-75,270,728 HK2, LINC01291, 7 more genes
    nsv6693587copy number variation1nstd229human GRCh38 chr2: 74,598,755-74,998,174 , GRCh37.p13 chr2: 74,825,882-75,225,301 HK2, LINC01291, 10 more genes
    nsv6693567copy number variation1nstd229human GRCh38 chr2: 74,664,687-74,764,389 , GRCh37.p13 chr2: 74,891,814-74,991,516 LOC102724482, SEMA4F, 2 more genes
    nsv6692636copy number variation1nstd229human GRCh38 chr2: 74,632,966-74,678,963 , GRCh37.p13 chr2: 74,860,093-74,906,090 M1AP, SEMA4F
    nsv6692029copy number variation1nstd229human GRCh38 chr2: 74,679,001-74,686,400 , GRCh37.p13 chr2: 74,906,128-74,913,527 SEMA4F
    nsv6689421copy number variation1nstd229human GRCh38 chr2: 74,695,834-74,939,138 , GRCh37.p13 chr2: 74,922,961-75,166,265 LOC105374809, LINC01293, 6 more genes
    nsv6689149copy number variation1nstd229human GRCh38 chr2: 74,576,501-74,843,500 , GRCh37.p13 chr2: 74,803,628-75,070,627 LOC102724497, RPS28P5, 6 more genes
    nsv6688871copy number variation1nstd229human GRCh38 chr2: 74,663,515-74,968,281 , GRCh37.p13 chr2: 74,890,642-75,195,408 POLE4, LOC102724497, 7 more genes
    nsv6688508copy number variation1nstd229human GRCh38 chr2: 74,592,565-74,749,791 , GRCh37.p13 chr2: 74,819,692-74,976,918 LOC102724497, TVP23BP2, 4 more genes
    nsv6686673copy number variation1nstd229human GRCh38 chr2: 74,687,815-74,695,418 , GRCh37.p13 chr2: 74,914,942-74,922,545 SEMA4F
    nsv6684148copy number variation1nstd229human GRCh38 chr2: 74,665,837-74,753,522 , GRCh37.p13 chr2: 74,892,964-74,980,649 SEMA4F, LOC102724482, 2 more genes
    nsv6684086copy number variation1nstd229human GRCh38 chr2: 74,670,987-74,671,018 , GRCh37.p13 chr2: 74,898,114-74,898,145 SEMA4F
    nsv6681849copy number variation1nstd229human GRCh38 chr2: 74,593,093-75,089,574 , GRCh37.p13 chr2: 74,820,220-75,316,701 HK2, MIR5000, 12 more genes
    nsv6681277copy number variation1nstd229human GRCh38 chr2: 74,644,596-74,762,751 , GRCh37.p13 chr2: 74,871,723-74,989,878 RPS28P5, SEMA4F, 3 more genes
    nsv6679705copy number variation1nstd229human GRCh38 chr2: 74,570,301-74,724,400 , GRCh37.p13 chr2: 74,797,428-74,951,527 LOC102724497, M1AP, 3 more genes
    nsv6679672copy number variation1nstd229human GRCh38 chr2: 74,692,562-74,833,313 , GRCh37.p13 chr2: 74,919,689-75,060,440 RPS28P5, HK2, 3 more genes
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