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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148229copy number variation1nstd102humanPathogenic GRCh38 chr4: 2,904,667-42,963,232 , GRCh37.p13 chr4: 2,906,394-42,965,249 LINC01587, RN7SKP82, 509 more genes
    nsv7148161copy number variation1nstd102humanPathogenic GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194 SLIRPP2, STIM2-AS1, 659 more genes
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7137196copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-34,512,694 , GRCh38.p12 chr4: 68,453-34,511,072 ECM1P2, LOC105378240, 482 more genes
    nsv7098818copy number variation1nstd102humanPathogenic GRCh38 chr4: 11,399,082-38,137,335 , GRCh37.p13 chr4: 11,400,706-38,138,956 LOC105374542, PPARGC1A, 232 more genes
    nsv7098707complex chromosomal rearrangement6nstd230human GRCh37 chr4: 17,956,694-17,956,694 , GRCh37 chr4: 17,956,695-17,956,695 , GRCh37 chr4: 56,623,741-56,623,741 , GRCh37 chr4: 56,623,741-56,623,741 , GRCh37 chr5: 108,665,769-108,665,769 , GRCh37 chr5: 115,260,598-115,260,598 , GRCh37 chr18: 74,724,997-74,724,997 , GRCh37 chr18: 74,724,997-74,724,997 , GRCh37 chr18: 77,244,456-77,244,456 , GRCh37 chr18: 77,244,456-77,244,456 , GRCh37 chr21: 20,191,089-20,191,089 , GRCh37 chr21: 20,191,091-20,191,091 , GRCh38.p12 chr18: 77,013,041-77,013,041 , GRCh38.p12 chr18: 77,013,041-77,013,041 , GRCh38.p12 chr18: 79,484,456-79,484,456 , GRCh38.p12 chr18: 79,484,456-79,484,456 , GRCh38.p12 chr21: 18,818,771-18,818,771 , GRCh38.p12 chr21: 18,818,773-18,818,773 , GRCh38.p12 chr4: 17,955,071-17,955,071 , GRCh38.p12 chr4: 17,955,072-17,955,072 , GRCh38.p12 chr4: 55,757,575-55,757,575 , GRCh38.p12 chr4: 55,757,575-55,757,575 , GRCh38.p12 chr5: 109,330,068-109,330,068 , GRCh38.p12 chr5: 115,924,901-115,924,901 , GRCh38.p12 chr4|NT_187541.1: 83,764-83,764 , GRCh38.p12 chr4|NT_187541.1: 83,764-83,764 MBP, NFATC1, 1 more genes
    nsv7053890inversion1nstd229human GRCh38 chr4: 16,156,227-18,504,313 , GRCh37.p13 chr4: 16,157,850-18,505,936 TAPT1, NCAPG, 26 more genes
    nsv7047237inversion1nstd229human GRCh38 chr4: 15,975,453-25,472,708 , GRCh37.p13 chr4: 15,977,076-25,474,330 LOC107986219, LOC102723675, 78 more genes
    nsv7044499inversion1nstd229human GRCh38 chr4: 16,435,218-18,199,516 , GRCh37.p13 chr4: 16,436,841-18,201,139 NACAP5, NCAPG, 19 more genes
    nsv6737572copy number variation1nstd229human GRCh38 chr4: 17,986,572-17,989,720 , GRCh37.p13 chr4: 17,988,195-17,991,343 LCORL
    nsv6737484copy number variation1nstd229human GRCh38 chr4: 17,971,732-18,022,868 , GRCh37.p13 chr4: 17,973,355-18,024,491 LCORL
    nsv6734134copy number variation1nstd229human GRCh38 chr4: 17,890,704-17,893,166 , GRCh37.p13 chr4: 17,892,327-17,894,789 LCORL
    nsv6730870copy number variation1nstd229human GRCh38 chr4: 17,859,855-17,864,292 , GRCh37.p13 chr4: 17,861,478-17,865,915 LCORL
    nsv6727125copy number variation1nstd229human GRCh38 chr4: 17,901,201-17,906,300 , GRCh37.p13 chr4: 17,902,824-17,907,923 LCORL
    nsv6725076copy number variation1nstd229human GRCh38 chr4: 17,850,519-17,853,384 , GRCh37.p13 chr4: 17,852,142-17,855,007 LCORL
    nsv6724347copy number variation1nstd229human GRCh38 chr4: 17,991,807-18,001,395 , GRCh37.p13 chr4: 17,993,430-18,003,018 LCORL
    nsv6722472copy number variation1nstd229human GRCh38 chr4: 17,976,968-17,977,061 , GRCh37.p13 chr4: 17,978,591-17,978,684 LCORL
    nsv6720579copy number variation1nstd229human GRCh38 chr4: 17,894,077-17,896,561 , GRCh37.p13 chr4: 17,895,700-17,898,184 LCORL
    nsv6719252copy number variation1nstd229human GRCh38 chr4: 18,001,230-18,005,843 , GRCh37.p13 chr4: 18,002,853-18,007,466 LCORL
    nsv6718334copy number variation1nstd229human GRCh38 chr4: 17,980,718-17,982,290 , GRCh37.p13 chr4: 17,982,341-17,983,913 LCORL
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