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Items: 1 to 20 of 206

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5921993copy number variation1nstd209human GRCh38 chr10: 90,979,234-99,692,336 , GRCh37.p13 chr10: 92,738,991-101,452,093 , CYP2C115P, 166 more genes
    nsv5913480copy number variation1nstd209human GRCh38 chr10: 99,685,982-99,687,238 , GRCh37.p13 chr10: 101,445,739-101,446,995 ENTPD7
    nsv5863063copy number variation1nstd209human GRCh38 chr10: 99,685,994-99,687,493 , GRCh37.p13 chr10: 101,445,751-101,447,250 ENTPD7
    nsv5694390mobile element insertion2nstd211human GRCh38 chr10: 99,678,069-99,678,069 , GRCh37.p13 chr10: 101,437,826-101,437,826 ENTPD7
    nsv5491258copy number variation1nstd206human GRCh38 chr10: 99,685,982-99,687,266 , GRCh37.p13 chr10: 101,445,739-101,447,023 ENTPD7
    nsv5489549copy number variation1nstd206human GRCh38 chr10: 99,661,966-99,688,450 , GRCh37.p13 chr10: 101,421,723-101,448,207 ENTPD7
    nsv5487031copy number variation1nstd206human GRCh38 chr10: 99,671,306-99,671,368 , GRCh37.p13 chr10: 101,431,063-101,431,125 ENTPD7
    nsv5408634mobile element insertion1nstd206human GRCh38 chr10: 99,678,069-99,678,120 , GRCh37.p13 chr10: 101,437,826-101,437,877 ENTPD7
    nsv5354429translocation1nstd200human GRCh38 chr10: 99,707,783-99,707,783 , GRCh38 chr10: 99,707,852-99,707,852 , GRCh37.p13 chr10: 101,467,609-101,467,609 , GRCh37.p13 chr10: 101,467,540-101,467,540 COX15, ENTPD7
    nsv5347286translocation1nstd200human GRCh38 chr10: 99,695,171-99,695,171 , GRCh38 chr7: 99,117,624-99,117,624 , GRCh37.p13 chr10: 101,454,928-101,454,928 , GRCh37.p13 chr7: 98,715,247-98,715,247 COX15, ENTPD7, 1 more genes
    nsv5347285translocation1nstd200human GRCh38 chr10: 99,694,800-99,694,800 , GRCh38 chr7: 99,117,371-99,117,371 , GRCh37.p13 chr10: 101,454,557-101,454,557 , GRCh37.p13 chr7: 98,714,994-98,714,994 COX15, ENTPD7, 1 more genes
    nsv5318710copy number variation1nstd204human GRCh38.p13 chr10: 99,661,962-99,688,459 , GRCh37.p13 chr10: 101,421,719-101,448,216 ENTPD7
    nsv5256490copy number variation1nstd204human GRCh38.p13 chr10: 99,661,653-99,688,561 , GRCh37.p13 chr10: 101,421,410-101,448,318 ENTPD7
    nsv5120463mobile element insertion1nstd203human GRCh38 chr10: 99,678,052-99,678,069 , GRCh37.p13 chr10: 101,437,809-101,437,826 ENTPD7
    nsv4970267copy number variation1nstd200human GRCh38 chr10: 99,661,966-99,688,450 , GRCh37.p13 chr10: 101,421,723-101,448,207 ENTPD7
    nsv4829446copy number variation1nstd200human GRCh37 chr10: 101,421,723-101,448,207 , GRCh38.p12 chr10: 99,661,966-99,688,450 ENTPD7
    nsv4672620copy number variation1nstd186human GRCh37 chr10: 101,445,703-101,446,976 , GRCh38.p12 chr10: 99,685,946-99,687,219 ENTPD7
    nsv4669782copy number variation1nstd186human GRCh37 chr10: 101,445,739-101,446,996 , GRCh38.p12 chr10: 99,685,982-99,687,239 ENTPD7
    nsv4616801copy number variation1nstd183human GRCh37 chr10: 101,445,739-101,446,996 , GRCh38.p12 chr10: 99,685,982-99,687,239 ENTPD7
    nsv4611396copy number variation1nstd183human GRCh37 chr10: 101,445,704-101,446,943 , GRCh38.p12 chr10: 99,685,947-99,687,186 ENTPD7
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