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Items: 1 to 20 of 832

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137115copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,467,726-29,044,717 , GRCh38.p12 chr16: 21,456,405-29,033,396 OTOAP1, GGA2, 148 more genes
    nsv7076939inversion1nstd229human GRCh38 chr16: 15,569,413-22,730,334 , GRCh37.p13 chr16: 15,663,270-22,741,655 ACSM5P1, RNU6-213P, 154 more genes
    nsv7075153inversion1nstd229human GRCh38 chr16: 21,267,353-22,312,593 , GRCh37.p13 chr16: 21,278,674-22,323,914 LOC100420536, LOC646828, 32 more genes
    nsv7074804inversion1nstd229human GRCh38 chr16: 21,265,744-22,316,509 , GRCh37.p13 chr16: 21,277,065-22,327,830 SMG1P4, LOC646828, 32 more genes
    nsv7067843inversion1nstd229human GRCh38 chr16: 21,291,198-22,687,975 , GRCh37.p13 chr16: 21,302,519-22,699,296 SMG1P4, NPIPB5, 41 more genes
    nsv7066172inversion1nstd229human GRCh38 chr16: 21,576,182-22,802,537 , GRCh37.p13 chr16: 21,587,503-22,813,858 UQCRC2, VWA3A, 31 more genes
    nsv7062907inversion1nstd229human GRCh38 chr16: 21,501,792-22,437,451 , GRCh37.p13 chr16: 21,513,113-22,448,772 LOC100420536, RRN3P3, 31 more genes
    nsv7060613inversion1nstd229human GRCh38 chr16: 21,590,269-22,770,847 , GRCh37.p13 chr16: 21,601,590-22,782,168 LOC105371129, OTOAP1, 31 more genes
    nsv7058720inversion1nstd229human GRCh38 chr16: 21,529,628-23,453,946 , GRCh37.p13 chr16: 21,540,949-23,465,267 CDR2-DT, LOC105371131, 40 more genes
    nsv7058493inversion1nstd229human GRCh38 chr16: 21,334,980-22,395,842 , GRCh37.p13 chr16: 21,346,301-22,407,163 LOC101927814, METTL9, 32 more genes
    nsv6993037copy number variation1nstd229human GRCh38 chr16: 21,660,152-21,664,658 , GRCh37.p13 chr16: 21,671,473-21,675,979 OTOA
    nsv6988630copy number variation1nstd229human GRCh38 chr16: 21,686,719-21,688,180 , GRCh37.p13 chr16: 21,698,040-21,699,501 OTOA
    nsv6985189copy number variation1nstd229human GRCh38 chr16: 21,714,789-21,718,103 , GRCh37.p13 chr16: 21,726,110-21,729,424 OTOA
    nsv6985001copy number variation1nstd229human GRCh38 chr16: 21,724,454-21,724,485 , GRCh37.p13 chr16: 21,735,775-21,735,806 OTOA
    nsv6983346copy number variation1nstd229human GRCh38 chr16: 21,691,921-21,692,622 , GRCh37.p13 chr16: 21,703,242-21,703,943 OTOA
    nsv6978877copy number variation1nstd229human GRCh38 chr16: 21,668,111-21,670,357 , GRCh37.p13 chr16: 21,679,432-21,681,678 OTOA
    nsv6637633copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,576,803-30,177,240 , GRCh38.p12 chr16: 21,565,482-30,165,919 USP31, CA5AP1, 200 more genes
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 MIR6511B2, ACSM5, 535 more genes
    nsv6636154copy number variation1nstd102humanPathogenic GRCh38 chr16: 21,624,041-21,730,798 , GRCh37.p13 chr16: 21,635,362-21,742,119 RNU6-196P, IGSF6, 3 more genes
    nsv6635605copy number variation1nstd227human GRCh38.p12 chr16: 21,567,067-21,828,019 , GRCh37 chr16: 21,578,388-21,839,340 , GRCh38.p12 chr16|NW_017852933.1: 1,276,756-1,537,746 IGSF6, METTL9, 6 more genes
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