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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094548copy number variation1nstd102humanUncertain significance GRCh37 chr15: 63,335,029-63,358,098 , GRCh38.p12 chr15: 63,042,830-63,065,899 TPM1, TPM1-AS
    nsv7094547copy number variation1nstd102humanPathogenic GRCh37 chr15: 62,146,656-64,747,263 , GRCh38.p12 chr15: 61,854,457-64,455,064 C2CD4A, SNX22, 40 more genes
    nsv7094392copy number variation1nstd102humanUncertain significance GRCh37 chr15: 63,351,742-63,356,266 , GRCh38.p12 chr15: 63,059,543-63,064,067 TPM1
    nsv7071327inversion1nstd229human GRCh38 chr15: 55,806,321-63,352,065 , GRCh37.p13 chr15: 56,098,519-63,644,264 LOC107984805, TPM1-AS, 120 more genes
    nsv7065633inversion1nstd229human GRCh38 chr15: 63,059,573-63,059,726 , GRCh37.p13 chr15: 63,351,772-63,351,925 TPM1
    nsv6977571copy number variation1nstd229human GRCh38 chr15: 63,062,646-63,071,088 , GRCh37.p13 chr15: 63,354,845-63,363,287 TPM1
    nsv6977283copy number variation1nstd229human GRCh38 chr15: 63,048,708-63,056,984 , GRCh37.p13 chr15: 63,340,907-63,349,183 TPM1-AS, TPM1
    nsv6977050copy number variation1nstd229human GRCh38 chr15: 63,064,142-63,065,895 , GRCh37.p13 chr15: 63,356,341-63,358,094 TPM1
    nsv6974961copy number variation1nstd229human GRCh38 chr15: 63,053,314-63,053,384 , GRCh37.p13 chr15: 63,345,513-63,345,583 TPM1
    nsv6973593copy number variation1nstd229human GRCh38 chr15: 63,064,377-63,069,778 , GRCh37.p13 chr15: 63,356,576-63,361,977 TPM1
    nsv6969451copy number variation1nstd229human GRCh38 chr15: 63,043,903-63,043,994 , GRCh37.p13 chr15: 63,336,102-63,336,193 TPM1
    nsv6967934copy number variation1nstd229human GRCh38 chr15: 63,042,944-63,056,984 , GRCh37.p13 chr15: 63,335,143-63,349,183 TPM1, TPM1-AS
    nsv6966240copy number variation1nstd229human GRCh38 chr15: 63,043,832-63,056,982 , GRCh37.p13 chr15: 63,336,031-63,349,181 TPM1, TPM1-AS
    nsv6965979copy number variation1nstd229human GRCh38 chr15: 63,062,645-63,064,061 , GRCh37.p13 chr15: 63,354,844-63,356,260 TPM1
    nsv6960684copy number variation1nstd229human GRCh38 chr15: 62,287,754-63,705,691 , GRCh37.p13 chr15: 62,579,953-63,997,890 MIR8067, RPS27L, 21 more genes
    nsv6958987copy number variation1nstd229human GRCh38 chr15: 63,046,344-63,046,695 , GRCh37.p13 chr15: 63,338,543-63,338,894 TPM1-AS, TPM1
    nsv6637384copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,589,845-63,543,438 , GRCh38.p12 chr15: 48,297,648-63,251,239 LINC03065, FAM227B, 228 more genes
    nsv6623275copy number variation1nstd224human GRCh37 chr15: 62,788,601-63,353,451 , GRCh38.p12 chr15: 62,496,402-63,061,252 TPM1, TLN2, 6 more genes
    nsv6309631copy number variation1nstd102humanUncertain significance GRCh37 chr15: 62,146,656-63,358,098 , GRCh38.p12 chr15: 61,854,457-63,065,899 HMGN1P26, VPS13C-DT, 17 more genes
    nsv6271481copy number variation1nstd214human GRCh38 chr15: 63,048,313-63,048,378 , GRCh37.p13 chr15: 63,340,512-63,340,577 TPM1-AS, TPM1
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