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Items: 1 to 20 of 108

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145947insertion1nstd232human GRCh37.p13 chr19: 49,930,971-49,930,971 , GRCh38.p12 chr19: 49,427,714-49,427,714 SLC17A7, GFY
    nsv7075539inversion1nstd229human GRCh38 chr19: 48,377,786-50,073,353 , GRCh37.p13 chr19: 48,881,043-50,576,610 SNRNP70, PTOV1, 126 more genes
    nsv7075255inversion1nstd229human GRCh38 chr19: 49,270,356-54,089,823 , GRCh37.p13 chr19: 49,773,613-54,528,887 FPR2, SNAR-A11, 344 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
    nsv7007960copy number variation1nstd229human GRCh38 chr19: 49,423,348-49,426,246 , GRCh37.p13 chr19: 49,926,605-49,929,503 PTH2, GFY
    nsv6597675inversion1nstd223human GRCh38 chr19: 49,424,371-49,426,087 , GRCh37.p13 chr19: 49,927,628-49,929,344 GFY
    nsv6595834inversion1nstd223human GRCh38 chr19: 48,004,600-50,148,749 , GRCh37.p13 chr19: 48,507,857-50,652,006 KDELR1, VRK3, 155 more genes
    nsv6531479copy number variation1nstd223human GRCh38 chr19: 49,427,821-49,429,237 , GRCh37.p13 chr19: 49,931,078-49,932,494 SLC17A7, GFY
    nsv6530855copy number variation1nstd223human GRCh38 chr19: 49,423,348-49,426,245 , GRCh37.p13 chr19: 49,926,605-49,929,502 PTH2, GFY
    nsv6526168copy number variation1nstd223human GRCh38 chr19: 49,416,354-49,424,404 , GRCh37.p13 chr19: 49,919,611-49,927,661 KASH5, GFY, 1 more genes
    nsv6313906copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 49,911,081-53,127,438 , GRCh38.p12 chr19: 49,407,824-52,624,185 AP2A1, KLK3, 212 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
    nsv6239078insertion1nstd214human GRCh38 chr19: 49,427,714-49,427,714 , GRCh37.p13 chr19: 49,930,971-49,930,971 GFY, SLC17A7
    nsv6207551copy number variation1nstd214human GRCh38 chr19: 49,429,078-49,429,257 , GRCh37.p13 chr19: 49,932,335-49,932,514 GFY, SLC17A7
    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
    nsv6112602insertion1nstd212human GRCh38 chr19: 49,427,730-49,427,730 , GRCh37.p13 chr19: 49,930,987-49,930,987 SLC17A7, GFY
    nsv6110571inversion1nstd212human GRCh38 chr19: 47,903,487-50,091,196 , GRCh37.p13 chr19: 48,406,744-50,594,453 , AP2A1, 155 more genes
    nsv6109339insertion1nstd212human GRCh38 chr19: 49,429,136-49,429,136 , GRCh37.p13 chr19: 49,932,393-49,932,393 GFY, SLC17A7
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