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Items: 1 to 20 of 135

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148095copy number variation1nstd102humanUncertain significance GRCh37 chr12: 121,341,598-124,103,434 , GRCh38.p12 chr12: 120,903,795-123,618,887 ANAPC5, MLXIP, 82 more genes
    nsv7094203copy number variation1nstd102humanUncertain significance GRCh37 chr12: 122,277,634-124,242,579 , GRCh38.p12 chr12: 121,839,728-123,758,032 SBNO1, MIR9902-1, 58 more genes
    nsv7058574inversion1nstd229human GRCh38 chr12: 122,435,128-123,376,948 , GRCh37.p13 chr12: 122,919,675-123,861,495 RNA5SP375, HCAR1, 23 more genes
    nsv6936937copy number variation1nstd229human GRCh38 chr12: 122,726,383-122,738,385 , GRCh37.p13 chr12: 123,210,930-123,222,932 HCAR1
    nsv6934866copy number variation1nstd229human GRCh38 chr12: 119,918,701-123,974,100 , GRCh37.p13 chr12: 120,356,505-124,458,647 RNU6-1088P, LOC105370042, 130 more genes
    nsv6934336copy number variation1nstd229human GRCh38 chr12: 122,713,201-122,741,900 , GRCh37.p13 chr12: 123,197,748-123,226,447 HCAR1, HCAR3
    nsv6929385copy number variation1nstd229human GRCh38 chr12: 122,720,603-122,726,575 , GRCh37.p13 chr12: 123,205,150-123,211,122 HCAR1
    nsv6924408copy number variation1nstd229human GRCh38 chr12: 122,644,242-123,080,927 , GRCh37.p13 chr12: 123,128,789-123,565,474 VPS37B, MIR9902-1, 13 more genes
    nsv6637402copy number variation1nstd102humanUncertain significance GRCh37 chr12: 122,737,779-123,265,478 , GRCh38.p12 chr12: 122,253,232-122,780,931 HCAR3, MIR9902-1, 13 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
    nsv6495235copy number variation1nstd223human GRCh38 chr12: 122,582,127-122,928,683 , GRCh37.p13 chr12: 123,066,674-123,413,230 MIR9902-2, VPS37B, 9 more genes
    nsv6486687copy number variation1nstd223human GRCh38 chr12: 122,555,650-122,786,484 , GRCh37.p13 chr12: 123,040,197-123,271,031 KNTC1, HCAR2, 6 more genes
    nsv6290266copy number variation1nstd102humanUncertain significance GRCh37 chr12: 121,887,337-123,386,068 , GRCh38.p12 chr12: 121,449,534-122,901,521 LINC02985, DENR, 38 more genes
    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
    nsv6132413copy number variation1nstd213human GRCh37 chr12: 121,590,000-123,620,001 , GRCh38.p12 chr12: 121,152,197-123,135,454 BCL7A, HPD, 51 more genes
    nsv5973346inversion1nstd209human GRCh38 chr12: 118,054,601-123,705,841 , GRCh37.p13 chr12: 118,492,406-124,190,388 , ACADS, 162 more genes
    nsv5927948copy number variation1nstd209human GRCh38 chr12: 122,731,120-122,741,826 , GRCh37.p13 chr12: 123,215,667-123,226,373 HCAR1
    nsv5864117copy number variation1nstd209human GRCh38 chr12: 122,731,141-122,736,584 , GRCh37.p13 chr12: 123,215,688-123,221,131 HCAR1
    nsv4996127copy number variation1nstd200human GRCh38 chr12: 122,723,215-122,724,698 , GRCh37.p13 chr12: 123,207,762-123,209,245 HCAR1
    nsv4847024copy number variation1nstd200human GRCh37 chr12: 123,215,666-123,226,374 , GRCh38.p12 chr12: 122,731,119-122,741,827 HCAR1
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