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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7038094inversion1nstd229human GRCh38 chr2: 106,480,616-110,213,336 , GRCh37.p13 chr2: 107,097,072-110,970,913 WASF1P1, LOC105373985, 72 more genes
    nsv6689607copy number variation1nstd229human GRCh38 chr2: 109,033,655-109,446,569 , GRCh37.p13 chr2: 109,650,111-110,063,025 SH3RF3-AS1, MIR4266, 3 more genes
    nsv6688899copy number variation1nstd229human GRCh38 chr2: 109,124,001-109,130,400 , GRCh37.p13 chr2: 109,740,457-109,746,856 SH3RF3, SH3RF3-AS1
    nsv6686545copy number variation1nstd229human GRCh38 chr2: 103,585,907-110,943,040 , GRCh37.p13 chr2: 104,202,365-111,700,617 PPP1R2P5, CAPZBP1, 142 more genes
    nsv6685842copy number variation1nstd229human GRCh38 chr2: 109,000,937-109,230,345 , GRCh37.p13 chr2: 109,617,393-109,846,801 SH3RF3-AS1, SH3RF3, 1 more genes
    nsv6685668copy number variation1nstd229human GRCh38 chr2: 109,118,764-109,127,597 , GRCh37.p13 chr2: 109,735,220-109,744,053 SH3RF3-AS1, SH3RF3
    nsv6684073copy number variation1nstd229human GRCh38 chr2: 109,125,976-109,128,057 , GRCh37.p13 chr2: 109,742,432-109,744,513 SH3RF3-AS1, SH3RF3
    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
    nsv6337683copy number variation1nstd223human GRCh38 chr2: 109,118,764-109,127,590 , GRCh37.p13 chr2: 109,735,220-109,744,046 SH3RF3, SH3RF3-AS1
    nsv6315410copy number variation1nstd102humanUncertain significance GRCh37 chr2: 108,446,955-110,504,318 , GRCh38.p12 chr2: 107,830,499-109,746,741 SULT1C3, SH3RF3-AS1, 37 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6315374copy number variation1nstd102humanPathogenic GRCh37 chr2: 109,157,562-110,497,991 , GRCh38.p12 chr2: 108,541,106-109,740,414 LOC105373545, LOC107985802, 19 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
    nsv6313505copy number variation1nstd102humanPathogenic GRCh37 chr2: 108,446,955-110,504,318 , GRCh38.p12 chr2: 107,830,499-109,746,741 SULT1C3, SH3RF3-AS1, 37 more genes
    nsv6291368copy number variation1nstd102humanUncertain significance GRCh37 chr2: 109,143,322-110,485,026 , GRCh38.p12 chr2: 108,526,866-109,727,449 GCC2-AS1, SH3RF3-AS1, 18 more genes
    nsv6290767copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 107,020,782-110,068,385 , GRCh38.p12 chr2: 106,404,326-109,451,929 CD8B2, LIMS1, 43 more genes
    nsv6134417copy number variation1nstd213human GRCh37 chr2: 109,360,000-110,870,001 , GRCh38.p12 chr2: 108,743,544-110,112,424 RANBP2, MALL, 34 more genes
    nsv6134137copy number variation1nstd213human GRCh37 chr2: 109,650,000-110,110,001 , GRCh38.p12 chr2: 109,033,544-109,492,881 SH3RF3, SH3RF3-AS1, 3 more genes
    nsv5985309copy number variation1nstd212human GRCh38 chr2: 108,715,210-112,293,808 , GRCh37.p13 chr2: 109,331,666-113,051,385 , NPHP1, 85 more genes
    nsv5667399inversion1nstd207human GRCh38 chr2: 108,527,822-109,733,036 , GRCh37.p13 chr2: 109,144,278-110,490,613 , LIMS1, 20 more genes
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