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Items: 1 to 20 of 129

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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
    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
    nsv6928853copy number variation1nstd229human GRCh38 chr12: 56,263,195-56,269,916 , GRCh37.p13 chr12: 56,656,979-56,663,700 CS, COQ10A
    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
    nsv6592389inversion1nstd223human GRCh38 chr12: 56,202,197-66,057,592 , GRCh37.p13 chr12: 56,595,981-66,451,372 RPL21P103, MIP, 194 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
    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
    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
    nsv6286034insertion1nstd214human GRCh38 chr12: 56,266,929-56,266,929 , GRCh37.p13 chr12: 56,660,713-56,660,713 COQ10A
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv5727618mobile element insertion1nstd211human GRCh38 chr12: 56,266,587-56,266,587 , GRCh37.p13 chr12: 56,660,371-56,660,371 COQ10A
    nsv5278526copy number variation1nstd204human GRCh38.p13 chr12: 55,839,801-56,299,500 , GRCh37.p13 chr12: 56,233,585-56,693,284 , NABP2, 30 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
    nsv4985646copy number variation1nstd200human GRCh38 chr12: 56,262,411-56,266,239 , GRCh37.p13 chr12: 56,656,195-56,660,023 COQ10A
    nsv4972871copy number variation1nstd200human GRCh38 chr12: 56,263,974-56,267,783 , GRCh37.p13 chr12: 56,657,758-56,661,567 COQ10A
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