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Items: 1 to 20 of 252

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6694223copy number variation1nstd229human GRCh38 chr2: 96,627,928-96,654,755 , GRCh37.p13 chr2: 97,293,665-97,320,492 FER1L5, KANSL3
    nsv6693559copy number variation1nstd229human GRCh38 chr2: 96,587,448-96,594,606 , GRCh37.p13 chr2: 97,253,185-97,260,343 KANSL3
    nsv6692356copy number variation1nstd229human GRCh38 chr2: 96,633,487-96,659,951 , GRCh37.p13 chr2: 97,299,224-97,325,688 KANSL3, FER1L5
    nsv6686507copy number variation1nstd229human GRCh38 chr2: 96,601,593-96,631,647 , GRCh37.p13 chr2: 97,267,330-97,297,384 KANSL3
    nsv6682513copy number variation1nstd229human GRCh38 chr2: 96,599,762-96,599,960 , GRCh37.p13 chr2: 97,265,499-97,265,697 KANSL3
    nsv6678338copy number variation1nstd229human GRCh38 chr2: 96,594,164-96,594,507 , GRCh37.p13 chr2: 97,259,901-97,260,244 KANSL3
    nsv6636315copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 95,341,388-100,340,514 , GRCh38.p12 chr2: 94,675,663-99,724,052 ADRA2B, ATP5F1BP1, 130 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6628429copy number variation1nstd224human GRCh37 chr2: 96,747,466-98,186,298 , GRCh38.p12 chr2: 96,081,718-97,569,835 ARID5A, IGKV2OR2-2, 42 more genes
    nsv6628179copy number variation1nstd224human GRCh37 chr2: 96,721,808-98,186,298 , GRCh38.p12 chr2: 96,056,060-97,569,835 ADRA2B, IGKV2OR2-10, 43 more genes
    nsv6548411inversion1nstd223human GRCh38 chr2: 96,614,332-96,614,513 , GRCh37.p13 chr2: 97,280,069-97,280,250 KANSL3
    nsv6547092inversion1nstd223human GRCh38 chr2: 96,007,660-97,097,743 , GRCh37.p13 chr2: 96,673,408-97,763,480 CNNM4, DUSP2, 34 more genes
    nsv6545790inversion1nstd223human GRCh38 chr2: 96,624,554-96,625,175 , GRCh37.p13 chr2: 97,290,291-97,290,912 KANSL3
    nsv6537497inversion1nstd223human GRCh38 chr2: 96,597,924-96,598,605 , GRCh37.p13 chr2: 97,263,661-97,264,342 KANSL3
    nsv6344662copy number variation1nstd223human GRCh38 chr2: 96,627,369-96,629,372 , GRCh37.p13 chr2: 97,293,106-97,295,109 KANSL3
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 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
    nsv6311431copy number variation1nstd102humanUncertain significance GRCh37 chr2: 96,780,545-97,475,254 , GRCh38.p12 chr2: 96,114,797-96,809,517 LOC105373496, STARD7-AS1, 17 more genes
    nsv6290784copy number variation1nstd102humanUncertain significance GRCh37 chr2: 96,544,603-98,025,634 , GRCh38.p12 chr2: 95,878,855-97,285,797 LOC100506076, FAHD2B, 39 more genes
    nsv6134374copy number variation1nstd213human GRCh37 chr2: 95,650,000-97,860,001 , GRCh38.p12 chr2: 94,984,255-97,194,264 ADRA2B, DUSP2, 68 more genes
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