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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148204copy number variation1nstd102humanPathogenic GRCh38 chr5: 9,999-14,320,000 , GRCh37.p13 chr5: 10,001-14,320,109 LOC105379638, LOC100420683, 185 more genes
    nsv7147550copy number variation1nstd232human GRCh37.p13 chr5: 211,061-211,149 , GRCh38.p12 chr5: 210,946-211,034 CCDC127
    nsv7146373copy number variation1nstd232human GRCh37.p13 chr5: 211,413-211,522 , GRCh38.p12 chr5: 211,298-211,407 CCDC127
    nsv7145922copy number variation1nstd232human GRCh37.p13 chr5: 211,341-211,408 , GRCh38.p12 chr5: 211,226-211,293 CCDC127
    nsv7143617copy number variation1nstd232human GRCh37.p13 chr5: 211,312-211,400 , GRCh38.p12 chr5: 211,197-211,285 CCDC127
    nsv7140705copy number variation1nstd232human GRCh37.p13 chr5: 196,752-196,835 , GRCh38.p12 chr5: 196,637-196,720 CCDC127, LRRC14B
    nsv7136971copy number variation1nstd102humanUncertain significance GRCh37 chr5: 218,337-257,198 , GRCh38.p12 chr5: 218,222-257,083 SDHA, CCDC127
    nsv7136965copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 218,337-236,542 , GRCh38.p12 chr5: 218,222-236,427 SDHA, CCDC127
    nsv7047634inversion1nstd229human GRCh38 chr5: 90,743-229,045 , GRCh37.p13 chr5: 90,858-229,160 CCDC127, LRRC14B, 2 more genes
    nsv7045728inversion1nstd229human GRCh38 chr5: 182,184-229,696 , GRCh37.p13 chr5: 182,299-229,811 CCDC127, LRRC14B, 2 more genes
    nsv7045668inversion1nstd229human GRCh38 chr5: 20,164-205,286 , GRCh37.p13 chr5: 20,164-205,401 CCDC127, LRRC14B, 3 more genes
    nsv7042391inversion1nstd229human GRCh38 chr5: 190,811-661,964 , GRCh37.p13 chr5: 190,926-662,079 LOC100310782, LOC105374606, 20 more genes
    nsv6776249copy number variation1nstd229human GRCh38 chr5: 191,265-303,477 , GRCh37.p13 chr5: 191,380-303,592 CCDC127, LRRC14B, 5 more genes
    nsv6772296copy number variation1nstd229human GRCh38 chr5: 105,167-310,399 , GRCh37.p13 chr5: 105,282-310,514 SDHA, PDCD6-DT, 6 more genes
    nsv6771095copy number variation1nstd229human GRCh38 chr5: 117,534-592,796 , GRCh37.p13 chr5: 117,649-592,911 SDHA, CCDC127, 17 more genes
    nsv6770308copy number variation1nstd229human GRCh38 chr5: 194,424-306,338 , GRCh37.p13 chr5: 194,539-306,453 CCDC127, LRRC14B, 5 more genes
    nsv6769967copy number variation1nstd229human GRCh38 chr5: 142,402-197,874 , GRCh37.p13 chr5: 142,517-197,989 CCDC127, LRRC14B, 1 more genes
    nsv6769260copy number variation1nstd229human GRCh38 chr5: 129,691-222,565 , GRCh37.p13 chr5: 129,806-222,680 SDHA, CCDC127, 2 more genes
    nsv6764776copy number variation1nstd229human GRCh38 chr5: 215,183-221,722 , GRCh37.p13 chr5: 215,298-221,837 SDHA, CCDC127
    nsv6762854copy number variation1nstd229human GRCh38 chr5: 95,146-200,737 , GRCh37.p13 chr5: 95,261-200,852 CCDC127, LRRC14B, 1 more genes
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