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Items: 1 to 20 of 152

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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
    nsv5672682copy number variation1nstd102humanPathogenic GRCh37 chr10: 101,478,103-101,478,257 , GRCh38.p12 chr10: 99,718,346-99,718,500 COX15
    nsv5493706copy number variation1nstd206human GRCh38 chr10: 99,728,233-99,730,847 , GRCh37.p13 chr10: 101,487,990-101,490,604 COX15, CUTC
    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
    nsv4541312insertion1nstd166human GRCh37.p13 chr10: 101,488,755-101,488,755 , GRCh38.p12 chr10: 99,728,998-99,728,998 COX15
    nsv4480306mobile element insertion1nstd166human GRCh37.p13 chr10: 101,481,127-101,481,127 , GRCh38.p12 chr10: 99,721,370-99,721,370 COX15
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4325673inversion1nstd166human GRCh37.p13 chr10: 92,228,734-107,785,320 , GRCh38.p12 chr10: 90,468,977-106,025,562 , COX15, 323 more genes
    nsv4178880copy number variation1nstd166human GRCh37.p13 chr10: 101,471,297-101,783,479 , GRCh38.p12 chr10: 99,711,540-100,023,722 ABCC2, COX15, 5 more genes
    nsv3971307copy number variation1nstd168human GRCh38 chr10: 99,644,283-99,693,958 , GRCh37.p13 chr10: 101,404,040-101,453,715 ENTPD7, COX15, 2 more genes
    nsv3921251copy number variation1nstd102humanUncertain significance GRCh37 chr10: 101,093,697-102,235,324 , NCBI36 chr10: 101,083,687-102,225,314 , GRCh38 chr10: 99,333,940-100,475,567 CUTC, COX15, 29 more genes
    nsv3920295copy number variation1nstd102humanPathogenic NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422 EIF2S2P3, CYP17A1-AS1, 895 more genes
    nsv3911966copy number variation1nstd102humanUncertain significance NCBI36 chr10: 101,466,071-101,749,704 , GRCh38 chr10: 99,716,324-99,999,957 , GRCh37 chr10: 101,476,081-101,759,714 NANOGP6, CUTC, 4 more genes
    nsv3911437copy number variation1nstd102humanPathogenic GRCh38 chr10: 93,181,201-101,356,779 , NCBI36 chr10: 94,930,948-103,106,526 , GRCh37 chr10: 94,940,958-103,116,536 SLF2, CUTC, 171 more genes
    nsv3911005copy number variation1nstd102humanUncertain significance GRCh37 chr10: 101,146,389-102,407,978 , NCBI36 chr10: 101,136,379-102,397,968 , GRCh38 chr10: 99,386,632-100,648,221 NDUFB8, MTATP8P4, 32 more genes
    nsv3909942copy number variation1nstd102humanPathogenic GRCh37 chr10: 96,872,364-118,383,651 , GRCh38 chr10: 95,112,607-116,776,637 , NCBI36 chr10: 96,862,354-118,526,138 LOC102723665, SFR1, 360 more genes
    nsv3907664copy number variation1nstd102humandrug response GRCh37 chr10: 42,347,406-135,534,747 , GRCh38.p12 chr10: 42,101,241-133,787,422 SHOC2, FAM245B, 1487 more genes
    nsv3906389copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996 LOC100419870, LOC102724439, 2105 more genes
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