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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147508copy number variation1nstd232human GRCh37.p13 chr6: 55,461,821-55,461,913 , GRCh38.p12 chr6: 55,597,023-55,597,115 HMGCLL1
    nsv7144725copy number variation1nstd232human GRCh37.p13 chr6: 55,307,806-55,307,872 , GRCh38.p12 chr6: 55,443,008-55,443,074 HMGCLL1
    nsv7053716inversion1nstd229human GRCh38 chr6: 55,575,595-55,628,182 , GRCh37.p13 chr6: 55,440,393-55,492,980 HMGCLL1
    nsv7051235inversion1nstd229human GRCh38 chr6: 55,470,163-55,489,533 , GRCh37.p13 chr6: 55,334,961-55,354,331 HMGCLL1
    nsv6797340copy number variation1nstd229human GRCh38 chr6: 55,463,401-55,465,800 , GRCh37.p13 chr6: 55,328,199-55,330,598 HMGCLL1
    nsv6795720copy number variation1nstd229human GRCh38 chr6: 55,436,845-55,447,614 , GRCh37.p13 chr6: 55,301,643-55,312,412 HMGCLL1
    nsv6795275copy number variation1nstd229human GRCh38 chr6: 55,443,011-55,443,075 , GRCh37.p13 chr6: 55,307,809-55,307,873 HMGCLL1
    nsv6794886copy number variation1nstd229human GRCh38 chr6: 55,548,783-55,553,096 , GRCh37.p13 chr6: 55,413,581-55,417,894 HMGCLL1
    nsv6793363copy number variation1nstd229human GRCh38 chr6: 55,494,301-55,499,800 , GRCh37.p13 chr6: 55,359,099-55,364,598 HMGCLL1
    nsv6791166copy number variation1nstd229human GRCh38 chr6: 55,029,689-55,791,128 , GRCh37.p13 chr6: 54,894,487-55,655,926 HCRTR2, HMGCLL1, 2 more genes
    nsv6791093copy number variation1nstd229human GRCh38 chr6: 55,502,894-55,507,912 , GRCh37.p13 chr6: 55,367,692-55,372,710 HMGCLL1
    nsv6790933copy number variation1nstd229human GRCh38 chr6: 54,897,901-55,582,500 , GRCh37.p13 chr6: 54,762,699-55,447,298 HCRTR2, HMGCLL1, 2 more genes
    nsv6790509copy number variation1nstd229human GRCh38 chr6: 55,471,071-55,471,221 , GRCh37.p13 chr6: 55,335,869-55,336,019 HMGCLL1
    nsv6788849copy number variation1nstd229human GRCh38 chr6: 55,478,735-55,482,710 , GRCh37.p13 chr6: 55,343,533-55,347,508 HMGCLL1
    nsv6788537copy number variation1nstd229human GRCh38 chr6: 55,467,194-55,472,952 , GRCh37.p13 chr6: 55,331,992-55,337,750 HMGCLL1
    nsv6788527copy number variation1nstd229human GRCh38 chr6: 55,599,615-55,606,277 , GRCh37.p13 chr6: 55,464,413-55,471,075 HMGCLL1
    nsv6787431copy number variation1nstd229human GRCh38 chr6: 55,575,309-55,594,457 , GRCh37.p13 chr6: 55,440,107-55,459,255 HMGCLL1
    nsv6786508copy number variation1nstd229human GRCh38 chr6: 55,606,407-55,612,684 , GRCh37.p13 chr6: 55,471,205-55,477,482 HMGCLL1
    nsv6786385copy number variation1nstd229human GRCh38 chr6: 55,576,853-55,669,257 , GRCh37.p13 chr6: 55,441,651-55,534,055 HMGCLL1
    nsv6785737copy number variation1nstd229human GRCh38 chr6: 55,491,234-55,496,897 , GRCh37.p13 chr6: 55,356,032-55,361,695 HMGCLL1
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