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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148056copy number variation1nstd102humanPathogenic GRCh37 chr2: 186,698,504-223,918,111 , GRCh38.p12 chr2: 185,833,777-223,053,393 DNAJB1P1, MTCO2P17, 580 more genes
    nsv7050515inversion1nstd229human GRCh38 chr2: 191,406,034-191,406,064 , GRCh37.p13 chr2: 192,270,760-192,270,790 MYO1B
    nsv7049508inversion1nstd229human GRCh38 chr2: 191,348,796-191,366,270 , GRCh37.p13 chr2: 192,213,522-192,230,996 MYO1B
    nsv6697530copy number variation1nstd229human GRCh38 chr2: 191,357,329-191,357,737 , GRCh37.p13 chr2: 192,222,055-192,222,463 MYO1B
    nsv6696343copy number variation1nstd229human GRCh38 chr2: 191,325,501-191,332,500 , GRCh37.p13 chr2: 192,190,227-192,197,226 MYO1B
    nsv6693922copy number variation1nstd229human GRCh38 chr2: 191,270,567-191,274,761 , GRCh37.p13 chr2: 192,135,293-192,139,487 MYO1B
    nsv6692804copy number variation1nstd229human GRCh38 chr2: 191,129,557-191,470,123 , GRCh37.p13 chr2: 191,994,283-192,334,849 STAT4, LOC105373804, 3 more genes
    nsv6689691copy number variation1nstd229human GRCh38 chr2: 191,351,470-191,354,449 , GRCh37.p13 chr2: 192,216,196-192,219,175 MYO1B
    nsv6688557copy number variation1nstd229human GRCh38 chr2: 191,363,483-191,365,252 , GRCh37.p13 chr2: 192,228,209-192,229,978 MYO1B
    nsv6687504copy number variation1nstd229human GRCh38 chr2: 190,894,701-192,994,500 , GRCh37.p13 chr2: 191,759,427-193,859,226 LOC107985785, NABP1, 19 more genes
    nsv6686137copy number variation1nstd229human GRCh38 chr2: 191,240,970-191,244,336 , GRCh37.p13 chr2: 192,105,696-192,109,062 MYO1B
    nsv6685750copy number variation1nstd229human GRCh38 chr2: 191,253,317-191,261,265 , GRCh37.p13 chr2: 192,118,043-192,125,991 MYO1B
    nsv6685119copy number variation1nstd229human GRCh38 chr2: 191,424,675-191,431,091 , GRCh37.p13 chr2: 192,289,401-192,295,817 MYO1B
    nsv6681310copy number variation1nstd229human GRCh38 chr2: 191,237,260-191,294,879 , GRCh37.p13 chr2: 192,101,986-192,159,605 MYO1B
    nsv6681151copy number variation1nstd229human GRCh38 chr2: 191,364,844-191,364,897 , GRCh37.p13 chr2: 192,229,570-192,229,623 MYO1B
    nsv6678428copy number variation1nstd229human GRCh38 chr2: 191,328,747-191,331,137 , GRCh37.p13 chr2: 192,193,473-192,195,863 MYO1B
    nsv6678288copy number variation1nstd229human GRCh38 chr2: 191,299,466-191,302,000 , GRCh37.p13 chr2: 192,164,192-192,166,726 MYO1B
    nsv6637127copy number variation1nstd102humanPathogenic GRCh37 chr2: 189,909,904-209,468,383 , GRCh38.p12 chr2: 189,045,178-208,603,658 LOC100421409, LOC100507443, 310 more genes
    nsv6636571copy number variation1nstd102humanPathogenic GRCh37 chr2: 187,152,754-199,960,525 , GRCh38.p12 chr2: 186,288,027-199,095,802 GAPDHP59, OSGEPL1-AS1, 135 more genes
    nsv6627745copy number variation1nstd224human GRCh37 chr2: 192,214,895-192,326,034 , GRCh38.p12 chr2: 191,350,169-191,461,308 MYO1B, RNU6-1045P
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