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Items: 1 to 20 of 176

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145104insertion1nstd232human GRCh37.p13 chr19: 49,588,893-49,588,893 , GRCh38.p12 chr19: 49,085,636-49,085,636 SNRNP70
    nsv7142789copy number variation1nstd232human GRCh37.p13 chr19: 49,610,967-49,611,048 , GRCh38.p12 chr19: 49,107,710-49,107,791 SNRNP70
    nsv7095217copy number variation1nstd102humanUncertain significance GRCh37 chr19: 49,472,545-49,714,755 , GRCh38.p12 chr19: 48,969,288-49,211,498 NTF6A, CGB2, 25 more genes
    nsv7075539inversion1nstd229human GRCh38 chr19: 48,377,786-50,073,353 , GRCh37.p13 chr19: 48,881,043-50,576,610 SNRNP70, PTOV1, 126 more genes
    nsv7074377inversion1nstd229human GRCh38 chr19: 41,965,396-49,981,454 , GRCh37.p13 chr19: 42,514,712-50,484,711 IGFL1, SYMPK, 400 more genes
    nsv7064020inversion1nstd229human GRCh38 chr19: 48,004,601-50,148,757 , GRCh37.p13 chr19: 48,507,858-50,652,014 TEAD2, LHB, 155 more genes
    nsv7059446inversion1nstd229human GRCh38 chr19: 49,105,048-49,105,112 , GRCh37.p13 chr19: 49,608,305-49,608,369 SNRNP70
    nsv7017410copy number variation1nstd229human GRCh38 chr19: 49,104,736-49,107,622 , GRCh37.p13 chr19: 49,607,993-49,610,879 SNRNP70
    nsv7009237copy number variation1nstd229human GRCh38 chr19: 49,091,058-49,091,795 , GRCh37.p13 chr19: 49,594,315-49,595,052 SNRNP70
    nsv7002191copy number variation1nstd229human GRCh38 chr19: 49,098,704-49,101,389 , GRCh37.p13 chr19: 49,601,961-49,604,646 SNRNP70
    nsv6998924copy number variation1nstd229human GRCh38 chr19: 49,079,689-49,084,942 , GRCh37.p13 chr19: 49,582,946-49,588,199 SNRNP70, RN7SL708P
    nsv6597576inversion1nstd223human GRCh38 chr19: 49,093,094-49,093,680 , GRCh37.p13 chr19: 49,596,351-49,596,937 SNRNP70
    nsv6595834inversion1nstd223human GRCh38 chr19: 48,004,600-50,148,749 , GRCh37.p13 chr19: 48,507,857-50,652,006 KDELR1, VRK3, 155 more genes
    nsv6310544copy number variation1nstd102humanUncertain significance GRCh37 chr19: 49,519,325-50,366,015 , GRCh38.p12 chr19: 49,016,068-49,862,758 CGB5, MED25, 76 more genes
    nsv6133706copy number variation1nstd213human GRCh37 chr19: 49,520,000-50,090,001 , GRCh38.p12 chr19: 49,016,743-49,586,744 CD37, CGB3, 51 more genes
    nsv6133704copy number variation1nstd213human GRCh37 chr19: 45,030,000-55,230,001 , GRCh38.p12 chr19: 44,525,967-54,071,460 AP2A1, APOC1, 582 more genes
    nsv6133703copy number variation1nstd213human GRCh37 chr19: 41,220,000-49,640,001 , GRCh38.p12 chr19: 40,714,095-49,136,744 , APOC1, 402 more genes
    nsv6133474copy number variation1nstd213human GRCh37 chr19: 42,350,000-49,650,001 , GRCh38.p12 chr19: 41,845,937-49,146,744 , APOC1, 343 more genes
    nsv6110571inversion1nstd212human GRCh38 chr19: 47,903,487-50,091,196 , GRCh37.p13 chr19: 48,406,744-50,594,453 , AP2A1, 155 more genes
    nsv6103535insertion1nstd212human GRCh38 chr19: 49,092,919-49,092,919 , GRCh37.p13 chr19: 49,596,176-49,596,176 SNRNP70
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