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Items: 1 to 20 of 113

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147552insertion1nstd232human GRCh37.p13 chr10: 103,921,420-103,921,420 , GRCh38.p12 chr10: 102,161,663-102,161,663 NOLC1
    nsv7147017insertion1nstd232human GRCh37.p13 chr10: 103,912,287-103,912,287 , GRCh38.p12 chr10: 102,152,530-102,152,530 NOLC1
    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
    nsv7069326inversion1nstd229human GRCh38 chr10: 102,162,270-102,178,083 , GRCh37.p13 chr10: 103,922,027-103,937,840 NOLC1
    nsv7062124inversion1nstd229human GRCh38 chr10: 102,162,266-102,175,170 , GRCh37.p13 chr10: 103,922,023-103,934,927 NOLC1
    nsv7061391inversion1nstd229human GRCh38 chr10: 100,357,388-105,969,995 , GRCh37.p13 chr10: 102,117,145-107,729,753 , CALHM1, 127 more genes
    nsv7059886inversion1nstd229human GRCh38 chr10: 95,520,399-102,687,169 , GRCh37.p13 chr10: 97,280,156-104,446,926 , ENTPD1-AS1, 168 more genes
    nsv6580228inversion1nstd223human GRCh38 chr10: 102,162,266-102,175,170 , GRCh37.p13 chr10: 103,922,023-103,934,927 NOLC1
    nsv6454718copy number variation1nstd223human GRCh38 chr10: 102,148,863-102,152,999 , GRCh37.p13 chr10: 103,908,620-103,912,756 NOLC1, PPRC1
    nsv6454310copy number variation1nstd223human GRCh38 chr10: 102,155,250-102,156,022 , GRCh37.p13 chr10: 103,915,007-103,915,779 NOLC1
    nsv6440568copy number variation1nstd223human GRCh38 chr10: 102,154,928-102,157,716 , GRCh37.p13 chr10: 103,914,685-103,917,473 NOLC1
    nsv6131926copy number variation1nstd213human GRCh37 chr10: 103,560,000-105,280,001 , GRCh38.p12 chr10: 101,800,243-103,520,244 ARL3, CYP17A1, 56 more genes
    nsv5304042copy number variation1nstd204human GRCh38.p13 chr10: 101,912,568-102,213,549 , GRCh37.p13 chr10: 103,672,325-103,973,306 LDB1, PPRC1, 3 more genes
    nsv5257254copy number variation1nstd204human GRCh38.p13 chr10: 102,158,025-102,159,024 , GRCh37.p13 chr10: 103,917,782-103,918,781 NOLC1
    nsv5244983copy number variation1nstd204human GRCh38.p13 chr10: 101,912,601-102,213,600 , GRCh37.p13 chr10: 103,672,358-103,973,357 NOLC1, LDB1, 3 more genes
    nsv5138303mobile element insertion1nstd203human GRCh38 chr10: 102,158,332-102,158,346 , GRCh37.p13 chr10: 103,918,089-103,918,103 NOLC1
    nsv4973989copy number variation1nstd200human GRCh38 chr10: 102,148,863-102,152,999 , GRCh37.p13 chr10: 103,908,620-103,912,756 PPRC1, NOLC1
    nsv4970350copy number variation1nstd200human GRCh38 chr10: 102,154,928-102,157,716 , GRCh37.p13 chr10: 103,914,685-103,917,473 NOLC1
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