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Items: 1 to 20 of 186

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094683copy number variation1nstd102humanUncertain significance GRCh37 chr16: 65,821,800-72,146,396 , GRCh38.p12 chr16: 65,787,897-72,112,497 TRG-GCC5-1, RNU6-359P, 205 more genes
    nsv7094682copy number variation2nstd102humanPathogenic GRCh37 chr16: 65,821,800-67,208,957 , GRCh38.p12 chr16: 65,787,897-67,175,054 RNA5SP428, PHAF1, 38 more genes
    nsv7071424inversion1nstd229human GRCh38 chr16: 66,996,662-66,996,773 , GRCh37.p13 chr16: 67,030,565-67,030,676 CES4A
    nsv6990789copy number variation1nstd229human GRCh38 chr16: 66,987,263-66,990,208 , GRCh37.p13 chr16: 67,021,166-67,024,111 CES4A
    nsv6990340copy number variation1nstd229human GRCh38 chr16: 66,732,301-67,029,000 , GRCh37.p13 chr16: 66,766,204-67,062,903 DYNC1LI2-DT, NAE1, 14 more genes
    nsv6989514copy number variation1nstd229human GRCh38 chr16: 66,993,895-66,999,327 , GRCh37.p13 chr16: 67,027,798-67,033,230 CES4A
    nsv6987207copy number variation1nstd229human GRCh38 chr16: 67,000,252-67,003,547 , GRCh37.p13 chr16: 67,034,155-67,037,450 CES4A
    nsv6986833copy number variation1nstd229human GRCh38 chr16: 66,964,395-66,997,463 , GRCh37.p13 chr16: 66,998,298-67,031,366 CES4A, CES3
    nsv6984907copy number variation1nstd229human GRCh38 chr16: 66,984,318-66,988,956 , GRCh37.p13 chr16: 67,018,221-67,022,859 CES4A
    nsv6981596copy number variation1nstd229human GRCh38 chr16: 66,940,488-67,029,327 , GRCh37.p13 chr16: 66,974,391-67,063,230 LOC107984881, CES2, 4 more genes
    nsv6980858copy number variation1nstd229human GRCh38 chr16: 66,983,630-66,987,016 , GRCh37.p13 chr16: 67,017,533-67,020,919 CES4A
    nsv6979396copy number variation1nstd229human GRCh38 chr16: 66,841,465-67,115,793 , GRCh37.p13 chr16: 66,875,368-67,149,696 CBFB, CDH16, 11 more genes
    nsv6577032inversion1nstd223human GRCh38 chr16: 66,990,138-66,990,653 , GRCh37.p13 chr16: 67,024,041-67,024,556 CES4A
    nsv6510626copy number variation1nstd223human GRCh38 chr16: 66,986,078-66,999,612 , GRCh37.p13 chr16: 67,019,981-67,033,515 CES4A
    nsv6510191copy number variation1nstd223human GRCh38 chr16: 66,991,214-66,993,533 , GRCh37.p13 chr16: 67,025,117-67,027,436 CES4A
    nsv6508464copy number variation1nstd223human GRCh38 chr16: 67,008,596-67,010,742 , GRCh37.p13 chr16: 67,042,499-67,044,645 CES4A
    nsv6504402copy number variation1nstd223human GRCh38 chr16: 66,993,801-66,996,100 , GRCh37.p13 chr16: 67,027,704-67,030,003 CES4A
    nsv6503798copy number variation1nstd223human GRCh38 chr16: 66,987,992-66,991,227 , GRCh37.p13 chr16: 67,021,895-67,025,130 CES4A
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
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