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Items: 1 to 20 of 169

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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
    nsv7068356inversion1nstd229human GRCh38 chr10: 70,218,200-70,240,911 , GRCh37.p13 chr10: 71,977,956-72,000,667 PPA1
    nsv6887462copy number variation1nstd229human GRCh38 chr10: 70,231,296-70,231,635 , GRCh37.p13 chr10: 71,991,052-71,991,391 PPA1
    nsv6885510copy number variation1nstd229human GRCh38 chr10: 70,190,601-70,218,200 , GRCh37.p13 chr10: 71,950,357-71,977,956 PPA1, RPS25P9
    nsv6883132copy number variation1nstd229human GRCh38 chr10: 70,225,269-70,233,186 , GRCh37.p13 chr10: 71,985,025-71,992,942 PPA1
    nsv6593772inversion1nstd223human GRCh38 chr10: 70,215,038-70,215,677 , GRCh37.p13 chr10: 71,974,794-71,975,433 PPA1
    nsv6314185copy number variation1nstd102humanPathogenic GRCh37 chr10: 68,735,254-78,885,714 , GRCh38.p12 chr10: 66,975,496-77,125,956 SLC25A16, CTNNA3, 204 more genes
    nsv6291213copy number variation1nstd102humanUncertain significance GRCh37 chr10: 71,754,361-72,399,690 , GRCh38.p12 chr10: 69,994,605-70,639,934 MACROH2A2, CEP57L1P1, 14 more genes
    nsv6136902translocation1nstd213human GRCh38.p12 chr10: 70,215,643-70,215,643 , GRCh38.p12 chr10: 73,106,265-73,106,265 , GRCh37 chr10: 74,866,023-74,866,023 , GRCh37 chr10: 71,975,399-71,975,399 PPA1
    nsv6131888copy number variation1nstd213human GRCh37 chr10: 71,890,000-72,730,001 , GRCh38.p12 chr10: 70,130,244-70,970,244 NPFFR1, TBATA, 18 more genes
    nsv6020338copy number variation1nstd212human GRCh38 chr10: 70,220,851-70,220,920 , GRCh37.p13 chr10: 71,980,607-71,980,676 PPA1
    nsv6012877copy number variation1nstd212human GRCh38 chr10: 70,220,590-70,220,671 , GRCh37.p13 chr10: 71,980,346-71,980,427 PPA1
    nsv6004184copy number variation1nstd212human GRCh38 chr10: 70,221,036-70,221,089 , GRCh37.p13 chr10: 71,980,792-71,980,845 PPA1
    nsv5635221insertion1nstd207human GRCh38 chr10: 70,206,893-70,206,893 , GRCh37.p13 chr10: 71,966,649-71,966,649 PPA1
    nsv5626708insertion1nstd207human GRCh38 chr10: 70,206,855-70,206,855 , GRCh37.p13 chr10: 71,966,611-71,966,611 PPA1
    nsv5591041copy number variation1nstd207human GRCh38 chr10: 70,220,934-70,221,044 , GRCh37.p13 chr10: 71,980,690-71,980,800 PPA1
    nsv5591001copy number variation1nstd207human GRCh38 chr10: 70,220,625-70,220,716 , GRCh37.p13 chr10: 71,980,381-71,980,472 PPA1
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4976414copy number variation1nstd200human GRCh38 chr10: 70,220,112-70,221,058 , GRCh37.p13 chr10: 71,979,868-71,980,814 PPA1
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