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Items: 1 to 20 of 111

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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
    nsv7093699copy number variation1nstd102humanUncertain significance GRCh37 chr10: 102,747,968-103,535,657 , GRCh38.p12 chr10: 100,988,211-101,775,900 RNY5P7, TLX1, 25 more genes
    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
    nsv6891906copy number variation1nstd229human GRCh38 chr10: 101,134,195-101,134,504 , GRCh37.p13 chr10: 102,893,952-102,894,261 TLX1, TLX1NB
    nsv6885171copy number variation1nstd229human GRCh38 chr10: 101,023,532-101,227,683 , GRCh37.p13 chr10: 102,783,289-102,987,440 LOC107984262, LINC01514, 9 more genes
    nsv6884847copy number variation1nstd229human GRCh38 chr10: 101,086,357-101,167,450 , GRCh37.p13 chr10: 102,846,114-102,927,207 TLX1, RNY5P7, 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
    nsv6450689copy number variation1nstd223human GRCh38 chr10: 101,136,430-101,167,629 , GRCh37.p13 chr10: 102,896,187-102,927,386 TLX1NB, RNY5P7, 1 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
    nsv5488859copy number variation1nstd206human GRCh38 chr10: 101,084,368-101,214,368 , GRCh37.p13 chr10: 102,844,125-102,974,125 TLX1, SMARCE1P7, 3 more genes
    nsv5320376copy number variation1nstd204human GRCh38.p13 chr10: 101,019,383-101,764,485 , GRCh37.p13 chr10: 102,779,140-103,524,242 , KAZALD1, 23 more genes
    nsv5246148copy number variation1nstd204human GRCh38.p13 chr10: 101,110,082-101,132,152 , GRCh37.p13 chr10: 102,869,839-102,891,909 TLX1, TLX1NB
    nsv4845784copy number variation1nstd200human GRCh37 chr10: 102,779,150-103,524,239 , GRCh38.p12 chr10: 101,019,393-101,764,482 , POLL, 23 more genes
    nsv4680797copy number variation1nstd189human GRCh37.p13 chr10: 102,835,750-103,653,301 , GRCh38.p12 chr10: 101,075,993-101,893,544 , FGF8, 28 more genes
    nsv4384550copy number variation1nstd173human GRCh37 chr10: 102,874,403-103,093,618 , GRCh38.p12 chr10: 101,114,646-101,333,861 LBX1, LOC105378453, 8 more genes
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