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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148243copy number variation1nstd102humanPathogenic GRCh38 chr7: 137,463,392-159,345,973 , GRCh37.p13 chr7: 137,148,138-159,128,663 MIR11400, TRBV24-1, 531 more genes
    nsv7148234copy number variation1nstd102humanLikely pathogenic GRCh38 chr7: 138,620,939-159,233,475 , GRCh37.p13 chr7: 138,305,684-159,026,165 AOC1, ALDH7A1P3, 515 more genes
    nsv7097864copy number variation1nstd102humanPathogenic GRCh37 chr7: 130,781,014-150,301,047 , GRCh38.p12 chr7: 131,096,255-150,603,959 NOBOX, FAM131B, 466 more genes
    nsv7057176inversion1nstd229human GRCh38 chr7: 142,200,564-149,795,026 , GRCh37.p13 chr7: 141,988,816-149,492,114 RN7SL72P, RPL32P17, 258 more genes
    nsv7051735inversion1nstd229human GRCh38 chr7: 142,037,473-144,135,486 , GRCh37.p13 chr7: 141,988,816-143,832,579 LOC105375546, TRBV21-1, 162 more genes
    nsv7049746inversion1nstd229human GRCh38 chr7: 143,132,164-144,147,382 , GRCh37.p13 chr7: 142,829,257-143,844,475 RPL26P24, EPHA1, 55 more genes
    nsv6636458copy number variation1nstd102humanPathogenic GRCh37 chr7: 131,779,213-149,042,734 , GRCh38.p12 chr7: 132,094,454-149,345,643 TRBD2, TRBV5-2, 403 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6291163copy number variation1nstd102humanPathogenic GRCh37 chr7: 133,851,002-159,119,707 , GRCh38.p12 chr7: 134,166,250-159,327,017 TRB, ZC3HAV1L, 579 more genes
    nsv6290262copy number variation1nstd102humanPathogenic GRCh37 chr7: 133,848,099-145,814,115 , GRCh38.p12 chr7: 134,163,347-146,117,023 TRBJ2-7, PRSS2, 341 more genes
    nsv6142900copy number variation1nstd206human GRCh38 chr7: 143,608,689-143,614,779 , GRCh37.p13 chr7: 143,305,782-143,311,872 LOC101928466, TCAF1P1
    nsv6142451copy number variation1nstd206human GRCh38 chr7: 143,608,950-143,614,000 , GRCh37.p13 chr7: 143,306,043-143,311,093 LOC101928466, TCAF1P1
    nsv6141678copy number variation1nstd206human GRCh38 chr7: 143,522,800-143,650,300 , GRCh37.p13 chr7: 143,219,893-143,347,393 EPHA1-AS1, TCAF2, 7 more genes
    nsv6135900copy number variation1nstd213human GRCh37 chr7: 142,330,000-143,440,001 , GRCh38.p12 chr7: 142,622,486-143,742,908 , EPHA1, 82 more genes
    nsv6121051copy number variation1nstd186human GRCh37 chr7: 143,298,895-143,299,149 , GRCh38.p12 chr7: 143,601,802-143,602,056 TCAF1P1
    nsv6063505insertion1nstd212human GRCh38 chr7: 143,602,043-143,602,043 , GRCh37.p13 chr7: 143,299,136-143,299,136 TCAF1P1
    nsv6061599insertion1nstd212human GRCh38 chr7: 143,601,785-143,601,785 , GRCh37.p13 chr7: 143,298,878-143,298,878 TCAF1P1
    nsv6015175copy number variation1nstd212human GRCh38 chr7: 143,601,831-143,601,941 , GRCh37.p13 chr7: 143,298,924-143,299,034 TCAF1P1
    nsv5640735insertion1nstd207human GRCh38 chr7: 143,601,790-143,601,790 , GRCh37.p13 chr7: 143,298,883-143,298,883 TCAF1P1
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