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Items: 1 to 20 of 127

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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
    nsv6935713copy number variation1nstd229human GRCh38 chr12: 122,151,101-122,188,700 , GRCh37.p13 chr12: 122,635,648-122,673,247 LRRC43, IL31
    nsv6935021copy number variation1nstd229human GRCh38 chr12: 122,167,968-122,171,661 , GRCh37.p13 chr12: 122,652,515-122,656,208 IL31, LRRC43
    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
    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
    nsv6919601copy number variation1nstd229human GRCh38 chr12: 122,107,448-122,190,892 , GRCh37.p13 chr12: 122,591,995-122,675,439 IL31, LRRC43, 1 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
    nsv6494979copy number variation1nstd223human GRCh38 chr12: 122,169,562-122,173,530 , GRCh37.p13 chr12: 122,654,109-122,658,077 IL31, LRRC43
    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
    nsv6132141copy number variation1nstd213human GRCh37 chr12: 122,590,000-122,870,001 , GRCh38.p12 chr12: 122,105,453-122,385,454 LOC101593348, LRRC43, 8 more genes
    nsv5973346inversion1nstd209human GRCh38 chr12: 118,054,601-123,705,841 , GRCh37.p13 chr12: 118,492,406-124,190,388 , ACADS, 162 more genes
    nsv5497826copy number variation1nstd206human GRCh38 chr12: 122,169,498-122,170,414 , GRCh37.p13 chr12: 122,654,045-122,654,961 LRRC43, IL31
    nsv5365251translocation1nstd200human GRCh38 chr12: 122,170,755-122,170,755 , GRCh38 chr12: 122,161,564-122,161,564 , GRCh37.p13 chr12: 122,646,111-122,646,111 , GRCh37.p13 chr12: 122,655,302-122,655,302 IL31, LRRC43
    nsv5336669translocation1nstd200human GRCh37 chr12: 122,646,111-122,646,111 , GRCh37 chr12: 122,655,302-122,655,302 , GRCh38.p12 chr12: 122,161,564-122,161,564 , GRCh38.p12 chr12: 122,170,755-122,170,755 IL31, LRRC43
    nsv5321503translocation1nstd204human GRCh37.p13 chr12: 122,655,302-122,655,302 , GRCh37.p13 chr12: 122,646,111-122,646,111 , GRCh38.p13 chr12: 122,161,564-122,161,564 , GRCh38.p13 chr12: 122,170,755-122,170,755 LRRC43, IL31
    nsv5279438copy number variation1nstd204human GRCh38.p13 chr12: 122,162,050-122,170,821 , GRCh37.p13 chr12: 122,646,597-122,655,368 LRRC43, IL31
    nsv5263897copy number variation1nstd204human GRCh38.p13 chr12: 122,161,801-122,170,700 , GRCh37.p13 chr12: 122,646,348-122,655,247 IL31, LRRC43
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