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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
    nsv7147689insertion1nstd232human GRCh37.p13 chr12: 123,001,978-123,001,978 , GRCh38.p12 chr12: 122,517,431-122,517,431 RSRC2
    nsv7140533insertion1nstd232human GRCh37.p13 chr12: 123,001,979-123,001,979 , GRCh38.p12 chr12: 122,517,432-122,517,432 RSRC2
    nsv7137349insertion1nstd232human GRCh37.p13 chr12: 122,999,775-122,999,775 , GRCh38.p12 chr12: 122,515,228-122,515,228 RSRC2
    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
    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
    nsv6932731copy number variation1nstd229human GRCh38 chr12: 122,525,308-122,525,340 , GRCh37.p13 chr12: 123,009,855-123,009,887 RSRC2, KNTC1
    nsv6931174copy number variation1nstd229human GRCh38 chr12: 122,498,337-122,506,641 , GRCh37.p13 chr12: 122,982,884-122,991,188 RSRC2, ZCCHC8
    nsv6923099copy number variation1nstd229human GRCh38 chr12: 122,497,201-122,504,500 , GRCh37.p13 chr12: 122,981,748-122,989,047 ZCCHC8, RSRC2
    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
    nsv6583999inversion1nstd223human GRCh38 chr12: 122,507,864-122,508,918 , GRCh37.p13 chr12: 122,992,411-122,993,465 RSRC2
    nsv6583876inversion1nstd223human GRCh38 chr12: 118,054,469-123,705,974 , GRCh37.p13 chr12: 118,492,274-124,190,521 RPL11P5, RPL17P37, 159 more genes
    nsv6580063inversion1nstd223human GRCh38 chr12: 122,509,949-122,510,303 , GRCh37.p13 chr12: 122,994,496-122,994,850 RSRC2
    nsv6487615copy number variation1nstd223human GRCh38 chr12: 122,525,799-122,526,120 , GRCh37.p13 chr12: 123,010,346-123,010,667 KNTC1, RSRC2
    nsv6487209copy number variation1nstd223human GRCh38 chr12: 122,498,337-122,506,641 , GRCh37.p13 chr12: 122,982,884-122,991,188 RSRC2, ZCCHC8
    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
    nsv6038609copy number variation1nstd212human GRCh38 chr12: 122,525,791-122,526,120 , GRCh37.p13 chr12: 123,010,338-123,010,667 RSRC2, KNTC1
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