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Items: 1 to 20 of 130

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094201copy number variation1nstd102humanUncertain significance GRCh37 chr12: 119,624,810-119,624,913 , GRCh38.p12 chr12: 119,187,005-119,187,108 HSPB8
    nsv7094200copy number variation1nstd102humanUncertain significance GRCh37 chr12: 119,617,118-119,624,913 , GRCh38.p12 chr12: 119,179,313-119,187,108 LOC107984440, HSPB8
    nsv7094030copy number variation1nstd102humanUncertain significance GRCh37 chr12: 119,631,484-119,631,663 , GRCh38.p12 chr12: 119,193,679-119,193,858 LOC100287653, HSPB8
    nsv6936621copy number variation1nstd229human GRCh38 chr12: 119,187,089-119,193,698 , GRCh37.p13 chr12: 119,624,894-119,631,503 LOC100287653, HSPB8
    nsv6932580copy number variation1nstd229human GRCh38 chr12: 119,192,304-119,196,639 , GRCh37.p13 chr12: 119,630,109-119,634,444 LOC100287653, HSPB8
    nsv6932080copy number variation1nstd229human GRCh38 chr12: 119,140,101-119,218,200 , GRCh37.p13 chr12: 119,577,906-119,656,005 LOC112268101, HSPB8, 5 more genes
    nsv6926303copy number variation1nstd229human GRCh38 chr12: 119,180,557-119,184,153 , GRCh37.p13 chr12: 119,618,362-119,621,958 HSPB8, LOC107984440
    nsv6922003copy number variation1nstd229human GRCh38 chr12: 119,037,498-119,572,209 , GRCh37.p13 chr12: 119,475,303-120,010,014 HSPB8, LOC105370021, 11 more genes
    nsv6918490copy number variation1nstd229human GRCh38 chr12: 119,194,866-119,203,944 , GRCh37.p13 chr12: 119,632,671-119,641,749 LOC100287653, HSPB8
    nsv6918154copy number variation1nstd229human GRCh38 chr12: 119,109,746-119,269,667 , GRCh37.p13 chr12: 119,547,551-119,707,472 SRRM4, LOC105370025, 7 more genes
    nsv6621409copy number variation1nstd224human GRCh37 chr12: 119,563,064-120,078,577 , GRCh38.p12 chr12: 119,125,259-119,640,772 HSPB8, LINC00934, 12 more genes
    nsv6583876inversion1nstd223human GRCh38 chr12: 118,054,469-123,705,974 , GRCh37.p13 chr12: 118,492,274-124,190,521 RPL11P5, RPL17P37, 159 more genes
    nsv6490297copy number variation1nstd223human GRCh38 chr12: 119,180,557-119,184,147 , GRCh37.p13 chr12: 119,618,362-119,621,952 HSPB8, LOC107984440
    nsv6484459copy number variation1nstd223human GRCh38 chr12: 119,194,866-119,203,937 , GRCh37.p13 chr12: 119,632,671-119,641,742 HSPB8, LOC100287653
    nsv6290239copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 117,461,902-133,841,395 , GRCh38.p12 chr12: 117,024,097-133,264,809 ACADS, BCL7A, 356 more genes
    nsv5973346inversion1nstd209human GRCh38 chr12: 118,054,601-123,705,841 , GRCh37.p13 chr12: 118,492,406-124,190,388 , ACADS, 162 more genes
    nsv5510251copy number variation1nstd206human GRCh38 chr12: 119,181,055-119,181,712 , GRCh37.p13 chr12: 119,618,860-119,619,517 HSPB8, LOC107984440
    nsv5380734copy number variation1nstd102humanUncertain significance GRCh37 chr12: 119,631,494-119,631,673 , GRCh38.p12 chr12: 119,193,689-119,193,868 LOC100287653, HSPB8
    nsv5319252copy number variation1nstd204human GRCh37.p13 chr12: 119,618,854-119,619,519 , GRCh38.p13 chr12: 119,181,049-119,181,714 LOC107984440, HSPB8
    nsv4995925copy number variation1nstd200human GRCh38 chr12: 119,181,055-119,181,712 , GRCh37.p13 chr12: 119,618,860-119,619,517 HSPB8, LOC107984440
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