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Items: 1 to 20 of 331

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147733insertion1nstd232human GRCh37.p13 chr1: 223,934,867-223,934,867 , GRCh38.p12 chr1: 223,747,165-223,747,165 CAPN2
    nsv7137494insertion1nstd232human GRCh37.p13 chr1: 223,947,182-223,947,182 , GRCh38.p12 chr1: 223,759,480-223,759,480 CAPN2
    nsv7099264copy number variation1nstd231human GRCh38.p12 chr1: 222,151,895-226,849,338 , GRCh37 chr1: 222,325,237-227,037,039 PARP1, CAPN2, 99 more genes
    nsv7038964inversion1nstd229human GRCh38 chr1: 223,741,216-223,741,233 , GRCh37.p13 chr1: 223,928,918-223,928,935 CAPN2
    nsv6677962copy number variation1nstd229human GRCh38 chr1: 223,635,121-223,764,260 , GRCh37.p13 chr1: 223,822,823-223,951,962 CAPN2, LOC105373046, 4 more genes
    nsv6677700copy number variation1nstd229human GRCh38 chr1: 223,737,805-223,741,159 , GRCh37.p13 chr1: 223,925,507-223,928,861 LOC105373046, CAPN2
    nsv6674990copy number variation1nstd229human GRCh38 chr1: 223,740,780-223,743,040 , GRCh37.p13 chr1: 223,928,482-223,930,742 CAPN2, LOC105373046
    nsv6670701copy number variation1nstd229human GRCh38 chr1: 223,753,984-223,759,529 , GRCh37.p13 chr1: 223,941,686-223,947,231 CAPN2
    nsv6663219copy number variation1nstd229human GRCh38 chr1: 223,771,939-223,774,833 , GRCh37.p13 chr1: 223,959,641-223,962,535 CAPN2, LOC105373041
    nsv6662475copy number variation1nstd229human GRCh38 chr1: 223,724,556-223,726,360 , GRCh37.p13 chr1: 223,912,258-223,914,062 CAPN2
    nsv6660727copy number variation1nstd229human GRCh38 chr1: 223,685,413-223,707,172 , GRCh37.p13 chr1: 223,873,115-223,894,874 LOC105373281, RNU6-1248P, 1 more genes
    nsv6660264copy number variation1nstd229human GRCh38 chr1: 223,758,233-223,763,228 , GRCh37.p13 chr1: 223,945,935-223,950,930 CAPN2
    nsv6659265copy number variation1nstd229human GRCh38 chr1: 223,741,435-223,741,461 , GRCh37.p13 chr1: 223,929,137-223,929,163 CAPN2
    nsv6659188copy number variation1nstd229human GRCh38 chr1: 223,775,187-223,775,251 , GRCh37.p13 chr1: 223,962,889-223,962,953 CAPN2
    nsv6659110copy number variation1nstd229human GRCh38 chr1: 223,709,023-223,716,212 , GRCh37.p13 chr1: 223,896,725-223,903,914 CAPN2
    nsv6638068copy number variation1nstd102humanassociation GRCh38 chr1: 208,430,918-228,938,006 , GRCh37.p13 chr1: 208,604,263-229,073,753 AURKAP1, TLR5, 372 more genes
    nsv6636736copy number variation1nstd102humanUncertain significance GRCh37 chr1: 221,325,488-225,804,228 , GRCh38.p12 chr1: 221,152,146-225,616,526 BROX, LINC02765, 77 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6540195inversion1nstd223human GRCh38 chr1: 216,397,966-226,054,144 , GRCh37.p13 chr1: 216,571,308-226,241,845 LOC105373046, CNIH3-AS1, 154 more genes
    nsv6333763copy number variation1nstd223human GRCh38 chr1: 223,724,556-223,726,353 , GRCh37.p13 chr1: 223,912,258-223,914,055 CAPN2
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