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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148098copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 121,890,923-122,473,333 , GRCh38.p12 chr12: 121,453,120-122,035,427 BCL7A, HPD, 14 more genes
    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
    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
    nsv6927281copy number variation1nstd229human GRCh38 chr12: 122,045,163-122,047,275 , GRCh37.p13 chr12: 122,483,069-122,485,181 BCL7A
    nsv6926381copy number variation1nstd229human GRCh38 chr12: 122,038,432-122,038,999 , GRCh37.p13 chr12: 122,476,338-122,476,905 BCL7A
    nsv6923424copy number variation1nstd229human GRCh38 chr12: 122,060,173-122,068,186 , GRCh37.p13 chr12: 122,498,079-122,506,092 LINC02985, BCL7A
    nsv6921855copy number variation1nstd229human GRCh38 chr12: 122,039,713-122,040,496 , GRCh37.p13 chr12: 122,477,619-122,478,402 BCL7A
    nsv6921699copy number variation1nstd229human GRCh38 chr12: 122,044,801-122,047,300 , GRCh37.p13 chr12: 122,482,707-122,485,206 BCL7A
    nsv6920920copy number variation1nstd229human GRCh38 chr12: 121,001,001-122,266,400 , GRCh37.p13 chr12: 121,438,804-122,750,947 BCL7A, KDM2B, 36 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
    nsv6493610copy number variation1nstd223human GRCh38 chr12: 122,020,201-122,023,200 , GRCh37.p13 chr12: 122,458,107-122,461,106 BCL7A
    nsv6486976copy number variation1nstd223human GRCh38 chr12: 122,039,145-122,040,365 , GRCh37.p13 chr12: 122,477,051-122,478,271 BCL7A
    nsv6485649copy number variation1nstd223human GRCh38 chr12: 122,045,220-122,046,053 , GRCh37.p13 chr12: 122,483,126-122,483,959 BCL7A
    nsv6478671copy number variation1nstd223human GRCh38 chr12: 122,044,801-122,047,300 , GRCh37.p13 chr12: 122,482,707-122,485,206 BCL7A
    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
    nsv5947394copy number variation1nstd209human GRCh38 chr12: 122,021,404-122,021,584 , GRCh37.p13 chr12: 122,459,310-122,459,490 BCL7A
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