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Items: 1 to 20 of 233

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144651copy number variation1nstd232human GRCh37.p13 chr2: 118,850,387-118,850,533 , GRCh38.p12 chr2: 118,092,811-118,092,957 INSIG2
    nsv7053866inversion1nstd229human GRCh38 chr2: 117,841,314-118,149,907 , GRCh37.p13 chr2: 118,598,890-118,907,483 INSIG2, LOC107985940, 6 more genes
    nsv7050777inversion1nstd229human GRCh38 chr2: 117,420,323-122,585,255 , GRCh37.p13 chr2: 118,177,899-123,342,831 LOC105373578, RPL17P15, 65 more genes
    nsv7049592inversion1nstd229human GRCh38 chr2: 117,787,675-118,130,160 , GRCh37.p13 chr2: 118,545,251-118,887,736 DDX18, LOC101929908, 7 more genes
    nsv7045341inversion1nstd229human GRCh38 chr2: 118,109,758-118,109,840 , GRCh37.p13 chr2: 118,867,334-118,867,416 INSIG2
    nsv7044064inversion1nstd229human GRCh38 chr2: 112,019,946-120,004,832 , GRCh37.p13 chr2: 112,777,523-120,762,408 LOC105373563, IL1A, 112 more genes
    nsv7042586inversion1nstd229human GRCh38 chr2: 111,572,275-118,829,502 , GRCh37.p13 chr2: 112,329,852-119,587,078 LOC105373579, NT5DC4, 103 more genes
    nsv6694675copy number variation1nstd229human GRCh38 chr2: 117,322,932-118,727,842 , GRCh37.p13 chr2: 118,080,508-119,485,418 RN7SL111P, LOC101927709, 12 more genes
    nsv6685947copy number variation1nstd229human GRCh38 chr2: 118,107,405-118,107,532 , GRCh37.p13 chr2: 118,864,981-118,865,108 INSIG2
    nsv6636871copy number variation1nstd102humanPathogenic GRCh37 chr2: 116,761,476-123,897,262 , GRCh38.p12 chr2: 116,003,900-123,139,686 LOC105373578, RPL17P15, 78 more genes
    nsv6553311inversion1nstd223human GRCh38 chr2: 113,382,126-121,687,299 , GRCh37.p13 chr2: 114,139,703-122,444,875 RPSAP23, CCDC93, 98 more genes
    nsv6537720inversion1nstd223human GRCh38 chr2: 118,090,097-118,091,443 , GRCh37.p13 chr2: 118,847,673-118,849,019 INSIG2
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314748copy number variation1nstd102humanPathogenic GRCh37 chr2: 112,475,655-145,691,999 , GRCh38.p12 chr2: 111,718,078-144,934,432 MED15P9, TMEM37, 474 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6313770copy number variation1nstd102humanPathogenic GRCh37 chr2: 113,188,197-128,144,700 , GRCh38.p12 chr2: 112,430,620-127,387,124 LOC105373575, RPS20P11, 174 more genes
    nsv6298183copy number variation1nstd186human GRCh37 chr2: 118,850,387-118,851,182 , GRCh38.p12 chr2: 118,092,811-118,093,606 INSIG2
    nsv6296300copy number variation1nstd186human GRCh37 chr2: 118,850,446-118,850,534 , GRCh38.p12 chr2: 118,092,870-118,092,958 INSIG2
    nsv6291353copy number variation1nstd102humanPathogenic GRCh37 chr2: 111,484,468-146,333,604 , GRCh38.p12 chr2: 110,726,891-145,576,036 LINC01120, LOC105373585, 490 more genes
    nsv6261507copy number variation1nstd214human GRCh38 chr2: 118,094,248-118,094,366 , GRCh37.p13 chr2: 118,851,824-118,851,942 INSIG2
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