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Items: 1 to 20 of 126

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5923466copy number variation1nstd209human GRCh38 chr10: 10,939,075-10,939,198 , GRCh37.p13 chr10: 10,981,038-10,981,161 CELF2, LINC00710
    nsv5599079copy number variation1nstd207human GRCh38 chr10: 10,939,075-10,939,198 , GRCh37.p13 chr10: 10,981,038-10,981,161 LINC00710, CELF2
    nsv5586737copy number variation1nstd207human GRCh38 chr10: 10,939,203-10,939,259 , GRCh37.p13 chr10: 10,981,166-10,981,222 CELF2, LINC00710
    nsv5381768copy number variation1nstd102humanPathogenic GRCh37 chr10: 9,137,489-17,227,168 , GRCh38.p12 chr10: 9,095,526-17,185,169 PROSER2, C1QL3, 110 more genes
    nsv5134056mobile element insertion1nstd203human GRCh38 chr10: 10,936,367-10,936,383 , GRCh37.p13 chr10: 10,978,330-10,978,346 LINC00710, CELF2
    nsv4973568copy number variation1nstd200human GRCh38 chr10: 10,937,249-10,939,570 , GRCh37.p13 chr10: 10,979,212-10,981,533 LINC00710, CELF2
    nsv4969618copy number variation1nstd200human GRCh38 chr10: 10,931,462-10,940,029 , GRCh37.p13 chr10: 10,973,425-10,981,992 , CELF2, 1 more genes
    nsv4839390copy number variation1nstd200human GRCh37 chr10: 10,979,212-10,981,533 , GRCh38.p12 chr10: 10,937,249-10,939,570 CELF2, LINC00710
    nsv4830272copy number variation1nstd200human GRCh37 chr10: 10,985,621-10,986,572 , GRCh38.p12 chr10: 10,943,658-10,944,609 LINC00710, CELF2
    nsv4748529copy number variation1nstd199human GRCh37 chr10: 10,981,050-10,981,174 , GRCh38.p12 chr10: 10,939,087-10,939,211 CELF2, LINC00710
    nsv4604545copy number variation1nstd183human GRCh37 chr10: 10,831,374-11,189,604 , GRCh38.p12 chr10: 10,789,411-11,147,641 , CELF2, 3 more genes
    nsv4480093mobile element insertion1nstd166human GRCh37.p13 chr10: 10,978,330-10,978,330 , GRCh38.p12 chr10: 10,936,367-10,936,367 CELF2, LINC00710
    nsv4455607copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,026-15,273,144 , GRCh38.p12 chr10: 54,086-15,231,145 LOC105376357, LINC02649, 264 more genes
    nsv4429559copy number variation1nstd174human GRCh37 chr10: 10,980,943-10,981,354 , GRCh38.p12 chr10: 10,938,980-10,939,391 LINC00710, CELF2
    nsv4418594copy number variation1nstd174human GRCh37 chr10: 10,981,102-10,981,312 , GRCh38.p12 chr10: 10,939,139-10,939,349 CELF2, LINC00710
    nsv4387258copy number variation1nstd173human GRCh37 chr10: 10,823,014-11,007,378 , GRCh38.p12 chr10: 10,781,051-10,965,415 , SFTA1P, 2 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv3966267copy number variation1nstd168human GRCh38 chr10: 10,944,347-10,972,480 , GRCh37.p13 chr10: 10,986,310-11,014,443 CELF2, LINC00710
    nsv3924406copy number variation1nstd102humanPathogenic GRCh38 chr10: 69,261-19,184,047 , GRCh37 chr10: 224,406-19,472,976 , NCBI36 chr10: 105,201-19,512,982 WDR37, LOC105376364, 302 more genes
    nsv3924010copy number variation1nstd102humanUncertain significance GRCh37 chr10: 10,792,862-11,755,048 , NCBI36 chr10: 10,832,868-11,795,054 , GRCh38 chr10: 10,750,899-11,713,049 SFTA1P, USP6NL, 10 more genes
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