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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147181copy number variation1nstd232human GRCh37.p13 chr12: 56,575,377-56,575,482 , GRCh38.p12 chr12: 56,181,593-56,181,698 SMARCC2
    nsv7147043copy number variation1nstd232human GRCh37.p13 chr12: 56,563,479-56,563,558 , GRCh38.p12 chr12: 56,169,695-56,169,774 SMARCC2
    nsv7138977copy number variation1nstd232human GRCh37.p13 chr12: 56,578,720-56,578,812 , GRCh38.p12 chr12: 56,184,936-56,185,028 SMARCC2
    nsv7074641inversion1nstd229human GRCh38 chr12: 52,659,002-59,632,575 , GRCh37.p13 chr12: 53,052,786-60,026,356 , LOC105369777, 292 more genes
    nsv7071931inversion1nstd229human GRCh38 chr12: 55,156,710-64,781,897 , GRCh37.p13 chr12: 55,550,494-65,175,677 ZBTB39, MIR548Z, 236 more genes
    nsv7065167inversion1nstd229human GRCh38 chr12: 55,524,684-56,392,713 , GRCh37.p13 chr12: 55,918,468-56,786,497 TMEM198B, BLOC1S1, 57 more genes
    nsv7060060inversion1nstd229human GRCh38 chr12: 55,500,913-56,344,820 , GRCh37.p13 chr12: 55,894,697-56,738,604 MYL6B, OR6C64P, 54 more genes
    nsv6926001copy number variation1nstd229human GRCh38 chr12: 56,162,312-56,162,886 , GRCh37.p13 chr12: 56,556,096-56,556,670 SMARCC2
    nsv6924653copy number variation1nstd229human GRCh38 chr12: 56,178,671-56,178,693 , GRCh37.p13 chr12: 56,572,455-56,572,477 SMARCC2
    nsv6924218copy number variation1nstd229human GRCh38 chr12: 55,714,201-56,819,900 , GRCh37.p13 chr12: 56,107,985-57,213,684 ESYT1, STAT2, 66 more genes
    nsv6588914inversion1nstd223human GRCh38 chr12: 55,524,684-56,392,758 , GRCh37.p13 chr12: 55,918,468-56,786,542 IL23A, RPL41, 57 more genes
    nsv6464693copy number variation1nstd223human GRCh38 chr12: 56,160,318-56,161,384 , GRCh37.p13 chr12: 56,554,102-56,555,168 MYL6, SMARCC2
    nsv6459301copy number variation1nstd223human GRCh38 chr12: 56,175,106-56,176,833 , GRCh37.p13 chr12: 56,568,890-56,570,617 SMARCC2
    nsv6459150copy number variation1nstd223human GRCh38 chr12: 56,188,070-56,188,737 , GRCh37.p13 chr12: 56,581,854-56,582,521 SMARCC2, TRS-CGA4-1, 1 more genes
    nsv6315199copy number variation1nstd102humanUncertain significance GRCh38 chr12: 55,986,511-56,885,590 , GRCh37.p13 chr12: 56,380,295-57,279,374 ERBB3, APOF, 47 more genes
    nsv6313979copy number variation1nstd102humanUncertain significance GRCh37 chr12: 56,333,262-57,010,442 , GRCh38.p12 chr12: 55,939,478-56,616,658 TRS-CGA4-1, ANKRD52, 42 more genes
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132699copy number variation1nstd213human GRCh37 chr12: 56,390,000-56,610,001 , GRCh38.p12 chr12: 55,996,216-56,216,217 MYL6, RPS26, 15 more genes
    nsv5941828copy number variation1nstd209human GRCh38 chr12: 56,167,897-56,167,950 , GRCh37.p13 chr12: 56,561,681-56,561,734 SMARCC2
    nsv5940808copy number variation1nstd209human GRCh38 chr12: 56,180,147-56,180,441 , GRCh37.p13 chr12: 56,573,931-56,574,225 SMARCC2
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