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Items: 1 to 20 of 254

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7093904copy number variation1nstd102humanUncertain significance GRCh37 chr10: 99,344,461-105,992,004 , GRCh38.p12 chr10: 97,584,704-104,232,246 ABCC2, LBX1-AS1, 160 more genes
    nsv7063197inversion1nstd229human GRCh38 chr10: 104,156,709-104,167,638 , GRCh37.p13 chr10: 105,916,467-105,927,396 CFAP43, LOC751602
    nsv7061391inversion1nstd229human GRCh38 chr10: 100,357,388-105,969,995 , GRCh37.p13 chr10: 102,117,145-107,729,753 , CALHM1, 127 more genes
    nsv6896042copy number variation1nstd229human GRCh38 chr10: 104,195,994-104,239,061 , GRCh37.p13 chr10: 105,955,752-105,998,819 MIR609, CFAP43
    nsv6891851copy number variation1nstd229human GRCh38 chr10: 103,994,859-104,941,952 , GRCh37.p13 chr10: 105,754,617-106,701,710 LOC105378464, GSTO1, 16 more genes
    nsv6891746copy number variation1nstd229human GRCh38 chr10: 104,079,778-104,153,317 , GRCh37.p13 chr10: 105,839,536-105,913,075 SFR1, CFAP43, 1 more genes
    nsv6891290copy number variation1nstd229human GRCh38 chr10: 104,215,092-104,290,475 , GRCh37.p13 chr10: 105,974,850-106,050,233 CFAP43, MIR609, 3 more genes
    nsv6885124copy number variation1nstd229human GRCh38 chr10: 104,210,254-104,210,649 , GRCh37.p13 chr10: 105,970,012-105,970,407 CFAP43
    nsv6884311copy number variation1nstd229human GRCh38 chr10: 104,100,632-104,131,671 , GRCh37.p13 chr10: 105,860,390-105,891,429 CFAP43, SFR1
    nsv6884159copy number variation1nstd229human GRCh38 chr10: 104,213,417-104,261,659 , GRCh37.p13 chr10: 105,973,175-106,021,417 GSTO1, CFAP43, 1 more genes
    nsv6880434copy number variation1nstd229human GRCh38 chr10: 103,302,516-106,977,869 , GRCh37.p13 chr10: 105,062,273-108,737,627 RNU11-3P, GSTO2, 48 more genes
    nsv6637523copy number variation1nstd102humanUncertain significance GRCh37 chr10: 105,015,345-105,911,204 , GRCh38.p12 chr10: 103,255,588-104,151,446 PCGF6, INA, 20 more genes
    nsv6586377inversion1nstd223human GRCh38 chr10: 104,136,020-104,136,559 , GRCh37.p13 chr10: 105,895,778-105,896,317 CFAP43
    nsv6585581inversion1nstd223human GRCh38 chr10: 104,232,787-104,233,344 , GRCh37.p13 chr10: 105,992,545-105,993,102 CFAP43
    nsv6583540inversion1nstd223human GRCh38 chr10: 104,224,241-104,224,484 , GRCh37.p13 chr10: 105,983,999-105,984,242 CFAP43
    nsv6455541copy number variation1nstd223human GRCh38 chr10: 104,170,070-104,170,773 , GRCh37.p13 chr10: 105,929,828-105,930,531 CFAP43
    nsv6455172copy number variation1nstd223human GRCh38 chr10: 104,229,401-104,234,900 , GRCh37.p13 chr10: 105,989,159-105,994,658 CFAP43
    nsv6452374copy number variation1nstd223human GRCh38 chr10: 104,208,676-104,209,076 , GRCh37.p13 chr10: 105,968,434-105,968,834 CFAP43
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