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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7072039inversion1nstd229human GRCh38 chr16: 79,903,600-82,537,648 , GRCh37.p13 chr16: 79,937,497-82,571,253 RN7SKP176, LOC105371357, 34 more genes
    nsv7071533inversion1nstd229human GRCh38 chr16: 80,801,188-81,170,379 , GRCh37.p13 chr16: 80,835,085-81,203,984 CDYL2, ATMIN, 9 more genes
    nsv7070808inversion1nstd229human GRCh38 chr16: 79,903,594-82,532,651 , GRCh37.p13 chr16: 79,937,491-82,566,256 DYNLRB2, RNU6-1191P, 34 more genes
    nsv7069467inversion1nstd229human GRCh38 chr16: 77,603,047-81,438,175 , GRCh37.p13 chr16: 77,636,944-81,471,780 ATMIN, WWOX, 39 more genes
    nsv7060501inversion1nstd229human GRCh38 chr16: 81,043,158-81,044,305 , GRCh37.p13 chr16: 81,076,763-81,077,910 ATMIN
    nsv6995938copy number variation1nstd229human GRCh38 chr16: 81,047,650-81,057,859 , GRCh37.p13 chr16: 81,081,255-81,091,464 ATMIN, C16orf46
    nsv6994608copy number variation1nstd229human GRCh38 chr16: 76,392,054-84,158,971 , GRCh37.p13 chr16: 76,425,951-84,192,576 , MAFTRR, 87 more genes
    nsv6993656copy number variation1nstd229human GRCh38 chr16: 80,348,419-81,288,034 , GRCh37.p13 chr16: 80,382,316-81,321,639 BCO1, RNU6-1191P, 13 more genes
    nsv6990079copy number variation1nstd229human GRCh38 chr16: 81,032,122-81,198,318 , GRCh37.p13 chr16: 81,065,727-81,231,923 C16orf46, RNU6-1191P, 6 more genes
    nsv6984896copy number variation1nstd229human GRCh38 chr16: 80,642,208-81,673,247 , GRCh37.p13 chr16: 80,676,105-81,706,852 RNU6-1191P, BCO1, 18 more genes
    nsv6983976copy number variation1nstd229human GRCh38 chr16: 80,966,228-81,785,439 , GRCh37.p13 chr16: 81,000,125-81,819,044 PLCG2, PPIAP51, 17 more genes
    nsv6980237copy number variation1nstd229human GRCh38 chr16: 81,012,701-81,051,600 , GRCh37.p13 chr16: 81,046,306-81,085,205 CENPN, ATMIN, 2 more genes
    nsv6978193copy number variation1nstd229human GRCh38 chr16: 80,848,368-81,065,884 , GRCh37.p13 chr16: 80,882,265-81,099,489 CENPN, ARLNC1, 4 more genes
    nsv6637185copy number variation1nstd102humanUncertain significance GRCh37 chr16: 80,896,302-81,152,918 , GRCh38.p12 chr16: 80,862,405-81,119,313 LOC105371361, PKD1L2, 8 more genes
    nsv6634465copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 71,610,276-90,354,753 , GRCh38.p12 chr16: 71,576,373-90,228,345 AP1G1, AFG3L1P, 349 more genes
    nsv6623774copy number variation1nstd224human GRCh37 chr16: 81,045,176-81,444,857 , GRCh38.p12 chr16: 81,011,571-81,411,252 GAN, BCO1, 9 more genes
    nsv6513815copy number variation1nstd223human GRCh38 chr16: 81,047,501-81,319,200 , GRCh37.p13 chr16: 81,081,106-81,352,805 GCSH, LOC105371361, 6 more genes
    nsv6510907copy number variation1nstd223human GRCh38 chr16: 81,030,501-81,039,200 , GRCh37.p13 chr16: 81,064,106-81,072,805 ATMIN, CENPN-AS1, 1 more genes
    nsv6509621copy number variation1nstd223human GRCh38 chr16: 81,035,201-81,038,100 , GRCh37.p13 chr16: 81,068,806-81,071,705 ATMIN, CENPN-AS1
    nsv6508490copy number variation1nstd223human GRCh38 chr16: 81,047,681-81,057,847 , GRCh37.p13 chr16: 81,081,286-81,091,452 C16orf46, ATMIN
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