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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148221copy number variation1nstd102humanPathogenic GRCh38 chr6: 150,905,553-158,511,926 , GRCh37.p13 chr6: 151,226,689-158,932,958 RNU6-824P, LOC105378067, 97 more genes
    nsv7054232inversion1nstd229human GRCh38 chr6: 151,531,808-151,557,766 , GRCh37.p13 chr6: 151,852,943-151,878,901 CCDC170
    nsv7042877inversion1nstd229human GRCh38 chr6: 149,723,719-152,206,487 , GRCh37.p13 chr6: 150,044,855-152,527,622 MTHFD1L, RAET1F, 48 more genes
    nsv7042383inversion1nstd229human GRCh38 chr6: 151,557,708-151,652,382 , GRCh37.p13 chr6: 151,878,843-151,973,517 ESR1, CCDC170, 2 more genes
    nsv7041422inversion1nstd229human GRCh38 chr6: 150,201,394-154,373,035 , GRCh37.p13 chr6: 150,522,530-154,694,169 MTHFD1L, MYCT1, 56 more genes
    nsv7039847inversion1nstd229human GRCh38 chr6: 151,578,074-151,579,610 , GRCh37.p13 chr6: 151,899,209-151,900,745 CCDC170
    nsv6817297copy number variation1nstd229human GRCh38 chr6: 151,370,892-151,716,763 , GRCh37.p13 chr6: 151,692,027-152,037,898 ARMT1, HSPA8P15, 6 more genes
    nsv6816545copy number variation1nstd229human GRCh38 chr6: 151,539,068-151,543,690 , GRCh37.p13 chr6: 151,860,203-151,864,825 CCDC170
    nsv6816139copy number variation1nstd229human GRCh38 chr6: 151,077,301-151,497,900 , GRCh37.p13 chr6: 151,398,437-151,819,035 LOC102723831, ARMT1, 13 more genes
    nsv6816076copy number variation1nstd229human GRCh38 chr6: 151,612,001-151,615,700 , GRCh37.p13 chr6: 151,933,136-151,936,835 CCDC170, LOC107986528, 1 more genes
    nsv6814804copy number variation1nstd229human GRCh38 chr6: 151,543,014-151,550,020 , GRCh37.p13 chr6: 151,864,149-151,871,155 CCDC170
    nsv6814591copy number variation1nstd229human GRCh38 chr6: 151,510,106-151,515,480 , GRCh37.p13 chr6: 151,831,241-151,836,615 CCDC170
    nsv6813051copy number variation1nstd229human GRCh38 chr6: 151,521,901-151,528,800 , GRCh37.p13 chr6: 151,843,036-151,849,935 CCDC170
    nsv6807402copy number variation1nstd229human GRCh38 chr6: 151,075,901-151,743,600 , GRCh37.p13 chr6: 151,397,037-152,064,735 RNU6-813P, ARMT1, 16 more genes
    nsv6804121copy number variation1nstd229human GRCh38 chr6: 151,531,555-154,379,823 , GRCh37.p13 chr6: 151,852,690-154,700,957 MTND4LP20, TUBB4BP7, 32 more genes
    nsv6804030copy number variation1nstd229human GRCh38 chr6: 151,531,801-151,652,400 , GRCh37.p13 chr6: 151,852,936-151,973,535 RNU6-813P, LOC107986528, 2 more genes
    nsv6803732copy number variation1nstd229human GRCh38 chr6: 151,530,293-151,530,811 , GRCh37.p13 chr6: 151,851,428-151,851,946 CCDC170
    nsv6800823copy number variation1nstd229human GRCh38 chr6: 151,544,558-151,551,372 , GRCh37.p13 chr6: 151,865,693-151,872,507 CCDC170
    nsv6631092copy number variation1nstd224human GRCh37 chr6: 151,857,472-151,907,195 , GRCh38.p12 chr6: 151,536,337-151,586,060 CCDC170
    nsv6631091copy number variation1nstd224human GRCh37 chr6: 151,686,905-151,859,314 , GRCh38.p12 chr6: 151,365,770-151,538,179 RMND1, ZBTB2, 3 more genes
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