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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096586copy number variation1nstd102humanUncertain significance GRCh37 chr2: 171,675,102-174,232,392 , GRCh38.p12 chr2: 170,818,592-173,367,664 RNU6-182P, DCAF17, 36 more genes
    nsv6697476copy number variation1nstd229human GRCh38 chr2: 172,441,193-172,445,455 , GRCh37.p13 chr2: 173,305,921-173,310,183 ITGA6
    nsv6696782copy number variation1nstd229human GRCh38 chr2: 172,433,250-172,440,458 , GRCh37.p13 chr2: 173,297,978-173,305,186 ITGA6
    nsv6696520copy number variation1nstd229human GRCh38 chr2: 172,504,018-172,504,058 , GRCh37.p13 chr2: 173,368,746-173,368,786 ITGA6
    nsv6692154copy number variation1nstd229human GRCh38 chr2: 172,421,901-172,427,500 , GRCh37.p13 chr2: 173,286,629-173,292,228 ITGA6
    nsv6691792copy number variation1nstd229human GRCh38 chr2: 172,486,972-172,487,079 , GRCh37.p13 chr2: 173,351,700-173,351,807 ITGA6
    nsv6684685copy number variation1nstd229human GRCh38 chr2: 172,506,261-172,506,339 , GRCh37.p13 chr2: 173,370,989-173,371,067 ITGA6
    nsv6681737copy number variation1nstd229human GRCh38 chr2: 172,487,547-172,496,479 , GRCh37.p13 chr2: 173,352,275-173,361,207 ITGA6
    nsv6680249copy number variation1nstd229human GRCh38 chr2: 172,405,569-172,449,989 , GRCh37.p13 chr2: 173,270,297-173,314,717 ITGA6
    nsv6680122copy number variation1nstd229human GRCh38 chr2: 172,437,879-172,438,603 , GRCh37.p13 chr2: 173,302,607-173,303,331 ITGA6
    nsv6353807copy number variation1nstd223human GRCh38 chr2: 172,437,765-172,439,739 , GRCh37.p13 chr2: 173,302,493-173,304,467 ITGA6
    nsv6352014copy number variation1nstd223human GRCh38 chr2: 172,504,015-172,504,054 , GRCh37.p13 chr2: 173,368,743-173,368,782 ITGA6
    nsv6344650copy number variation1nstd223human GRCh38 chr2: 172,441,193-172,445,454 , GRCh37.p13 chr2: 173,305,921-173,310,182 ITGA6
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6315160copy number variation1nstd102humanPathogenic GRCh37 chr2: 160,347,642-174,075,851 , GRCh38.p12 chr2: 159,491,131-173,211,123 EIF3EP3, FAP, 158 more genes
    nsv6315016copy number variation1nstd102humanPathogenic GRCh37 chr2: 171,524,396-178,694,337 , GRCh38.p12 chr2: 170,667,886-177,829,610 LOC105373746, HAGLROS, 136 more genes
    nsv6278238insertion1nstd214human GRCh38 chr2: 172,435,260-172,435,260 , GRCh37.p13 chr2: 173,299,988-173,299,988 ITGA6
    nsv6243468mobile element insertion1nstd215human GRCh38 chr2: 172,471,513-172,471,513 , GRCh37.p13 chr2: 173,336,241-173,336,241 ITGA6
    nsv6243467mobile element insertion1nstd215human GRCh38 chr2: 172,452,009-172,452,009 , GRCh37.p13 chr2: 173,316,737-173,316,737 ITGA6
    nsv6134500copy number variation1nstd213human GRCh37 chr2: 149,790,000-179,310,001 , GRCh38.p12 chr2: 148,934,069-178,445,274 , ACVR1, 394 more genes
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