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Items: 1 to 20 of 126

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098853copy number variation1nstd102humanUncertain significance GRCh37 chr2: 24,962,301-26,257,604 , GRCh38.p12 chr2: 24,739,432-26,034,735 TPM3P7, EFR3B, 25 more genes
    nsv7096625copy number variation1nstd102humanUncertain significance GRCh37 chr2: 24,443,763-30,143,525 , GRCh38.p12 chr2: 24,220,894-29,920,659 LOC105374381, POMC, 136 more genes
    nsv7096148copy number variation2nstd102humanUncertain significance GRCh37 chr2: 24,443,763-29,022,169 , GRCh38.p12 chr2: 24,220,894-28,799,303 LOC105374381, SLC35F6, 122 more genes
    nsv6676291copy number variation1nstd229human GRCh38 chr2: 25,805,489-25,809,255 , GRCh37.p13 chr2: 26,028,358-26,032,124 TPM3P7, ASXL2
    nsv6672785copy number variation1nstd229human GRCh38 chr2: 24,384,939-32,866,867 , GRCh37.p13 chr2: 24,607,808-33,091,934 CENPO, TOGARAM2, 170 more genes
    nsv6664717copy number variation1nstd229human GRCh38 chr2: 25,227,058-26,008,194 , GRCh37.p13 chr2: 25,449,927-26,231,063 TPM3P7, MIR1301, 9 more genes
    nsv6659142copy number variation1nstd229human GRCh38 chr2: 25,796,701-26,364,100 , GRCh37.p13 chr2: 26,019,570-26,586,968 KIF3C, ADGRF3, 18 more genes
    nsv6658810copy number variation1nstd229human GRCh38 chr2: 25,806,901-25,809,900 , GRCh37.p13 chr2: 26,029,770-26,032,769 TPM3P7, ASXL2
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 LOC105374455, RN7SL674P, 504 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
    nsv6543735inversion1nstd223human GRCh38 chr2: 24,403,241-32,916,237 , GRCh37.p13 chr2: 24,626,110-33,141,304 LOC105374334, LOC107985861, 172 more genes
    nsv6538559inversion1nstd223human GRCh38 chr2: 25,762,333-32,867,002 , GRCh37.p13 chr2: 25,985,202-33,092,069 MIR558, PCARE, 148 more genes
    nsv6344534copy number variation1nstd223human GRCh38 chr2: 24,831,925-32,916,230 , GRCh37.p13 chr2: 25,054,794-33,141,297 LOC102723594, DNAJC5G, 165 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6315162copy number variation1nstd102humannot provided GRCh37 chr2: 24,641,638-26,473,160 , GRCh38.p12 chr2: 24,418,769-26,250,292 RNU6-942P, RPS13P5, 37 more genes
    nsv6137788copy number variation1nstd102humanPathogenic GRCh37 chr2: 24,601,818-43,466,284 , GRCh38.p12 chr2: 24,378,949-43,239,145 GTF3C2-AS1, MAPRE3-AS1, 316 more genes
    nsv6112680copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 24,881,528-43,460,021 , GRCh38.p12 chr2: 24,658,659-43,232,882 ADCY3, ALK, 314 more genes
    nsv6047240insertion1nstd212human GRCh38 chr2: 25,807,532-25,807,532 , GRCh37.p13 chr2: 26,030,401-26,030,401 TPM3P7, ASXL2
    nsv5543531insertion1nstd206human GRCh38 chr2: 25,808,055-25,808,073 , GRCh37.p13 chr2: 26,030,924-26,030,942 ASXL2, TPM3P7
    nsv4728444copy number variation1nstd102humanUncertain significance GRCh37 chr2: 25,938,039-26,385,614 , GRCh38.p12 chr2: 25,715,170-26,162,745 SMARCE1P6, TRMT112P6, 13 more genes
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