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Items: 1 to 20 of 207

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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
    nsv7059886inversion1nstd229human GRCh38 chr10: 95,520,399-102,687,169 , GRCh37.p13 chr10: 97,280,156-104,446,926 , ENTPD1-AS1, 168 more genes
    nsv6893102copy number variation1nstd229human GRCh38 chr10: 100,247,809-100,292,406 , GRCh37.p13 chr10: 102,007,566-102,052,163 CWF19L1, BLOC1S2, 3 more genes
    nsv6595106inversion1nstd223human GRCh38 chr10: 92,377,901-102,079,487 , GRCh37.p13 chr10: 94,137,658-103,839,244 , ARHGAP19, 201 more genes
    nsv6593415inversion1nstd223human GRCh38 chr10: 100,265,085-100,265,284 , GRCh37.p13 chr10: 102,024,842-102,025,041 CWF19L1
    nsv6449827copy number variation1nstd223human GRCh38 chr10: 100,259,116-100,279,790 , GRCh37.p13 chr10: 102,018,873-102,039,547 BLOC1S2, RNU6-422P, 1 more genes
    nsv6442960copy number variation1nstd223human GRCh38 chr10: 100,242,691-100,243,405 , GRCh37.p13 chr10: 102,002,448-102,003,162 CWF19L1
    nsv6442660copy number variation1nstd223human GRCh38 chr10: 100,237,191-100,237,580 , GRCh37.p13 chr10: 101,996,948-101,997,337 SNORA12, CWF19L1
    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
    nsv6441110copy number variation1nstd223human GRCh38 chr10: 100,247,815-100,292,337 , GRCh37.p13 chr10: 102,007,572-102,052,094 PKD2L1, CWF19L1, 3 more genes
    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
    nsv6131925copy number variation2nstd213human GRCh37 chr10: 101,250,000-103,190,001 , GRCh38.p12 chr10: 99,490,243-101,430,244 CHUK, ABCC2, 52 more genes
    nsv6131845copy number variation1nstd213human GRCh37 chr10: 100,150,000-103,440,001 , GRCh38.p12 chr10: 98,390,243-101,680,244 CHUK, ABCC2, 70 more genes
    nsv6015562copy number variation1nstd212human GRCh38 chr10: 100,252,558-100,255,368 , GRCh37.p13 chr10: 102,012,315-102,015,125 CWF19L1
    nsv6010723copy number variation1nstd212human GRCh38 chr10: 100,231,216-100,245,042 , GRCh37.p13 chr10: 101,990,973-102,004,799 CWF19L1, SNORA12
    nsv5484206copy number variation1nstd206human GRCh38 chr10: 100,247,808-100,248,329 , GRCh37.p13 chr10: 102,007,565-102,008,086 CWF19L1, PHB1P9
    nsv5481050copy number variation1nstd206human GRCh38 chr10: 100,242,455-100,243,379 , GRCh37.p13 chr10: 102,002,212-102,003,136 CWF19L1
    nsv5348041translocation1nstd200human GRCh38 chr10: 100,247,808-100,247,808 , GRCh38 chr10: 100,248,329-100,248,329 , GRCh37.p13 chr10: 102,007,565-102,007,565 , GRCh37.p13 chr10: 102,008,086-102,008,086 PHB1P9, CWF19L1
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