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Items: 1 to 20 of 976

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097800copy number variation1nstd102humanPathogenic GRCh37 chr8: 55,537,210-55,542,913 , GRCh38.p12 chr8: 54,624,650-54,630,353 RP1
    nsv7093508insertion1nstd102humanPathogenic GRCh37 chr8: 55,540,527-55,540,527 , GRCh38 chr8: 54,627,967-54,627,967 RP1
    nsv7067508inversion1nstd229human GRCh38 chr8: 51,755,366-56,976,322 , GRCh37.p13 chr8: 52,667,926-57,888,881 CHCHD2P10, LOC105375850, 81 more genes
    nsv7064051inversion1nstd229human GRCh38 chr8: 53,370,406-56,357,942 , GRCh37.p13 chr8: 54,282,966-57,270,501 CHCHD2P10, RN7SL798P, 51 more genes
    nsv7059807inversion1nstd229human GRCh38 chr8: 54,849,906-54,864,977 , GRCh37.p13 chr8: 55,762,466-55,777,537 RP1
    nsv7058511inversion1nstd229human GRCh38 chr8: 54,860,697-54,891,312 , GRCh37.p13 chr8: 55,773,257-55,803,872 RP1
    nsv6857918copy number variation1nstd229human GRCh38 chr8: 54,593,761-54,599,673 , GRCh37.p13 chr8: 55,506,321-55,512,233 RP1
    nsv6857183copy number variation1nstd229human GRCh38 chr8: 54,656,501-54,670,400 , GRCh37.p13 chr8: 55,569,061-55,582,960 RP1
    nsv6856927copy number variation1nstd229human GRCh38 chr8: 54,817,245-54,817,968 , GRCh37.p13 chr8: 55,729,805-55,730,528 RP1
    nsv6856570copy number variation1nstd229human GRCh38 chr8: 54,549,323-54,572,269 , GRCh37.p13 chr8: 55,461,883-55,484,829 RP1
    nsv6856469copy number variation1nstd229human GRCh38 chr8: 54,720,570-54,784,021 , GRCh37.p13 chr8: 55,633,130-55,696,581 LOC105375842, RP1
    nsv6855850copy number variation1nstd229human GRCh38 chr8: 54,538,729-54,541,869 , GRCh37.p13 chr8: 55,451,289-55,454,429 RP1
    nsv6853848copy number variation1nstd229human GRCh38 chr8: 54,536,723-54,540,294 , GRCh37.p13 chr8: 55,449,283-55,452,854 RP1
    nsv6853661copy number variation1nstd229human GRCh38 chr8: 54,589,002-54,595,578 , GRCh37.p13 chr8: 55,501,562-55,508,138 RP1
    nsv6852705copy number variation1nstd229human GRCh38 chr8: 54,619,523-54,630,640 , GRCh37.p13 chr8: 55,532,083-55,543,200 RP1
    nsv6852368copy number variation1nstd229human GRCh38 chr8: 54,658,269-54,658,581 , GRCh37.p13 chr8: 55,570,829-55,571,141 RP1
    nsv6852114copy number variation1nstd229human GRCh38 chr8: 54,580,201-54,585,900 , GRCh37.p13 chr8: 55,492,761-55,498,460 RP1
    nsv6851915copy number variation1nstd229human GRCh38 chr8: 54,551,730-54,559,129 , GRCh37.p13 chr8: 55,464,290-55,471,689 RP1
    nsv6851904copy number variation1nstd229human GRCh38 chr8: 54,614,154-54,614,363 , GRCh37.p13 chr8: 55,526,714-55,526,923 RP1
    nsv6850979copy number variation1nstd229human GRCh38 chr8: 54,526,862-54,530,389 , GRCh37.p13 chr8: 55,439,422-55,442,949 RP1
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