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Items: 1 to 20 of 270

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7044080inversion1nstd229human GRCh38 chr2: 136,783,750-142,804,814 , GRCh37.p13 chr2: 137,541,320-143,562,383 LOC105373634, LOC107985822, 42 more genes
    nsv6697812copy number variation1nstd229human GRCh38 chr2: 137,995,241-138,000,879 , GRCh37.p13 chr2: 138,752,811-138,758,449 LOC107985948, HNMT
    nsv6697162copy number variation1nstd229human GRCh38 chr2: 137,341,754-138,049,253 , GRCh37.p13 chr2: 138,099,324-138,806,823 RNA5SP105, LOC105373634, 5 more genes
    nsv6693880copy number variation1nstd229human GRCh38 chr2: 137,980,762-137,982,655 , GRCh37.p13 chr2: 138,738,332-138,740,225 HNMT, LOC107985948
    nsv6693165copy number variation1nstd229human GRCh38 chr2: 137,915,119-138,032,155 , GRCh37.p13 chr2: 138,672,689-138,789,725 LOC101928273, LOC107985948, 1 more genes
    nsv6691605copy number variation1nstd229human GRCh38 chr2: 136,115,914-144,517,285 , GRCh37.p13 chr2: 136,873,484-145,274,852 LOC105373652, LOC105373649, 68 more genes
    nsv6690209copy number variation1nstd229human GRCh38 chr2: 136,466,024-140,671,797 , GRCh37.p13 chr2: 137,223,594-141,429,366 LRP1B, LOC101928273, 35 more genes
    nsv6686994copy number variation1nstd229human GRCh38 chr2: 136,848,278-138,281,224 , GRCh37.p13 chr2: 137,605,848-139,038,794 LOC101928273, LINC01832, 7 more genes
    nsv6686748copy number variation1nstd229human GRCh38 chr2: 137,995,301-138,000,900 , GRCh37.p13 chr2: 138,752,871-138,758,470 HNMT, LOC107985948
    nsv6685220copy number variation1nstd229human GRCh38 chr2: 137,985,378-137,987,366 , GRCh37.p13 chr2: 138,742,948-138,744,936 HNMT, LOC107985948
    nsv6685156copy number variation1nstd229human GRCh38 chr2: 137,992,877-138,000,898 , GRCh37.p13 chr2: 138,750,447-138,758,468 HNMT, LOC107985948
    nsv6684596copy number variation1nstd229human GRCh38 chr2: 137,826,711-138,402,498 , GRCh37.p13 chr2: 138,584,281-139,160,068 LOC101928273, IDI1P1, 6 more genes
    nsv6682241copy number variation1nstd229human GRCh38 chr2: 137,450,773-138,122,902 , GRCh37.p13 chr2: 138,208,343-138,880,472 LOC107985948, LOC105373634, 6 more genes
    nsv6681169copy number variation1nstd229human GRCh38 chr2: 137,977,801-137,979,100 , GRCh37.p13 chr2: 138,735,371-138,736,670 HNMT, LOC107985948
    nsv6680910copy number variation1nstd229human GRCh38 chr2: 137,935,379-137,974,228 , GRCh37.p13 chr2: 138,692,949-138,731,798 HNMT
    nsv6679692copy number variation1nstd229human GRCh38 chr2: 128,625,642-138,426,614 , GRCh37.p13 chr2: 129,383,216-139,184,184 MTND4P27, LOC646674, 194 more genes
    nsv6543671inversion1nstd223human GRCh38 chr2: 137,970,752-137,971,401 , GRCh37.p13 chr2: 138,728,322-138,728,971 HNMT
    nsv6354399copy number variation1nstd223human GRCh38 chr2: 138,008,152-138,008,549 , GRCh37.p13 chr2: 138,765,722-138,766,119 HNMT, LOC107985948
    nsv6346437copy number variation1nstd223human GRCh38 chr2: 138,014,401-138,015,200 , GRCh37.p13 chr2: 138,771,971-138,772,770 HNMT, LOC107985948
    nsv6345639copy number variation1nstd223human GRCh38 chr2: 137,990,737-137,992,105 , GRCh37.p13 chr2: 138,748,307-138,749,675 HNMT, LOC107985948
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