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Items: 1 to 20 of 112

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6933225copy number variation1nstd229human GRCh38 chr12: 56,585,982-56,590,732 , GRCh37.p13 chr12: 56,979,766-56,984,516 RBMS2, RNU6-343P
    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
    nsv6922441copy number variation1nstd229human GRCh38 chr12: 56,586,501-56,594,700 , GRCh37.p13 chr12: 56,980,285-56,988,484 RBMS2, RNU6-343P, 1 more genes
    nsv6592389inversion1nstd223human GRCh38 chr12: 56,202,197-66,057,592 , GRCh37.p13 chr12: 56,595,981-66,451,372 RPL21P103, MIP, 194 more genes
    nsv6584140inversion1nstd223human GRCh38 chr12: 56,381,670-66,057,684 , GRCh37.p13 chr12: 56,775,454-66,451,464 RNU6-879P, KICS2, 180 more genes
    nsv6578359inversion1nstd223human GRCh38 chr12: 56,201,986-66,057,683 , GRCh37.p13 chr12: 56,595,770-66,451,463 AVIL, RPSAP52, 194 more genes
    nsv6577024inversion1nstd223human GRCh38 chr12: 56,201,970-66,057,680 , GRCh37.p13 chr12: 56,595,754-66,451,460 AVPR1A, LOC390332, 194 more genes
    nsv6576885inversion1nstd223human GRCh38 chr12: 56,344,988-66,057,676 , GRCh37.p13 chr12: 56,738,772-66,451,456 LOC105369786, MBD6, 184 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
    nsv5280306copy number variation1nstd204human GRCh38.p13 chr12: 56,543,401-56,595,900 , GRCh37.p13 chr12: 56,937,185-56,989,684 RBMS2, BAZ2A, 1 more genes
    nsv5272629copy number variation1nstd204human GRCh38.p13 chr12: 56,586,850-56,602,716 , GRCh37.p13 chr12: 56,980,634-56,996,500 BAZ2A, RNU6-343P, 1 more genes
    nsv5267790copy number variation1nstd204human GRCh37.p13 chr12: 56,781,185-56,989,684 , GRCh38.p13 chr12: 56,387,401-56,595,900 MIP, RBMS2, 7 more genes
    nsv5266736copy number variation1nstd204human GRCh38.p13 chr12: 56,587,001-56,622,100 , GRCh37.p13 chr12: 56,980,785-57,015,884 RNU6-343P, BAZ2A, 1 more genes
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 , MIR6502, 769 more genes
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 , MYL6B, 769 more genes
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