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Items: 1 to 20 of 180

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144404insertion1nstd232human GRCh37.p13 chr10: 101,384,909-101,384,909 , GRCh38.p12 chr10: 99,625,152-99,625,152 SLC25A28, LOC105378450
    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
    nsv7076200inversion1nstd229human GRCh38 chr10: 99,636,051-99,637,683 , GRCh37.p13 chr10: 101,395,808-101,397,440 SLC25A28, LOC105378450
    nsv7059886inversion1nstd229human GRCh38 chr10: 95,520,399-102,687,169 , GRCh37.p13 chr10: 97,280,156-104,446,926 , ENTPD1-AS1, 168 more genes
    nsv6896966copy number variation1nstd229human GRCh38 chr10: 99,626,743-99,629,511 , GRCh37.p13 chr10: 101,386,500-101,389,268 LOC105378450, SLC25A28
    nsv6894989copy number variation1nstd229human GRCh38 chr10: 99,606,803-99,609,552 , GRCh37.p13 chr10: 101,366,560-101,369,309 SLC25A28
    nsv6891025copy number variation1nstd229human GRCh38 chr10: 99,654,956-99,659,956 , GRCh37.p13 chr10: 101,414,713-101,419,713 ENTPD7, SLC25A28
    nsv6888227copy number variation1nstd229human GRCh38 chr10: 99,642,969-99,645,448 , GRCh37.p13 chr10: 101,402,726-101,405,205 SLC25A28, LOC105378450
    nsv6888169copy number variation1nstd229human GRCh38 chr10: 99,626,363-99,633,809 , GRCh37.p13 chr10: 101,386,120-101,393,566 LOC105378450, SLC25A28
    nsv6884971copy number variation1nstd229human GRCh38 chr10: 99,630,100-99,630,574 , GRCh37.p13 chr10: 101,389,857-101,390,331 LOC105378450, SLC25A28
    nsv6881964copy number variation1nstd229human GRCh38 chr10: 99,645,866-99,659,747 , GRCh37.p13 chr10: 101,405,623-101,419,504 SLC25A28, LOC105378450, 1 more genes
    nsv6595106inversion1nstd223human GRCh38 chr10: 92,377,901-102,079,487 , GRCh37.p13 chr10: 94,137,658-103,839,244 , ARHGAP19, 201 more genes
    nsv6448107copy number variation1nstd223human GRCh38 chr10: 99,655,029-99,656,825 , GRCh37.p13 chr10: 101,414,786-101,416,582 SLC25A28
    nsv6444137copy number variation1nstd223human GRCh38 chr10: 99,607,741-99,609,971 , GRCh37.p13 chr10: 101,367,498-101,369,728 SLC25A28
    nsv6441680copy number variation1nstd223human GRCh38 chr10: 99,317,365-100,480,706 , GRCh37.p13 chr10: 101,077,122-102,240,463 WNT8B, GOT1, 29 more genes
    nsv6309049copy number variation1nstd102humanPathogenic GRCh37 chr10: 100,177,321-101,611,388 , GRCh38.p12 chr10: 98,417,564-99,851,631 SLC25A28, RPL7P36, 18 more genes
    nsv6281007insertion2nstd214human GRCh38 chr10: 99,625,152-99,625,152 , GRCh37.p13 chr10: 101,384,909-101,384,909 LOC105378450, SLC25A28
    nsv6132013copy number variation1nstd213human GRCh37 chr10: 101,250,000-103,200,001 , GRCh38.p12 chr10: 99,490,243-101,440,244 CHUK, ABCC2, 52 more genes
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