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Items: 1 to 20 of 106

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7068936inversion1nstd229human GRCh38 chr12: 75,617,673-76,899,935 , GRCh37.p13 chr12: 76,011,453-77,293,715 CSRP2, OSBPL8, 23 more genes
    nsv7068424inversion1nstd229human GRCh38 chr12: 75,621,086-76,899,941 , GRCh37.p13 chr12: 76,014,866-77,293,721 LOC100289143, LOC105369844, 23 more genes
    nsv6923571copy number variation1nstd229human GRCh38 chr12: 76,567,795-76,664,406 , GRCh37.p13 chr12: 76,961,575-77,058,186 LOC105369850, RPL21P98, 3 more genes
    nsv6587098inversion1nstd223human GRCh38 chr12: 70,939,082-79,478,721 , GRCh37.p13 chr12: 71,332,862-79,872,501 , H3P35, 83 more genes
    nsv6291127copy number variation1nstd102humanPathogenic GRCh37 chr12: 70,084,476-77,065,764 , GRCh38.p12 chr12: 69,690,696-76,671,984 LOC100130268, RNU6-1012P, 78 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
    nsv6132437copy number variation1nstd213human GRCh37 chr12: 75,550,000-78,060,001 , GRCh38.p12 chr12: 75,156,220-77,666,221 , CSRP2, 40 more genes
    nsv5500934copy number variation1nstd206human GRCh38 chr12: 76,069,603-82,449,398 , GRCh37.p13 chr12: 76,463,383-82,843,177 , E2F7, 65 more genes
    nsv5037136inversion1nstd200human GRCh38 chr12: 69,787,024-109,882,221 , GRCh37.p13 chr12: 70,180,804-110,320,026 , RPL23AP68, 540 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 , MIR6502, 769 more genes
    nsv5032581inversion1nstd200human GRCh38 chr12: 67,763,754-90,678,993 , GRCh37.p13 chr12: 68,157,534-91,072,770 , LOC105369886, 255 more genes
    nsv4888823inversion1nstd200human GRCh37 chr12: 68,157,543-91,072,771 , GRCh38.p12 chr12: 67,763,763-90,678,994 , BEST3, 255 more genes
    nsv4886161inversion1nstd200human GRCh37 chr12: 70,180,810-110,320,027 , GRCh38.p12 chr12: 69,787,030-109,882,222 , LOC728739, 540 more genes
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 , MYL6B, 769 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4345788sequence alteration1nstd166human GRCh37.p13 chr12: 59,785,153-101,478,055 , GRCh38.p12 chr12: 59,391,372-101,084,277 , APAF1, 538 more genes
    nsv4325802inversion1nstd166human GRCh37.p13 chr12: 70,180,810-110,320,028 , GRCh38.p12 chr12: 69,787,030-109,882,223 , APAF1, 540 more genes
    nsv4324772inversion1nstd166human GRCh37.p13 chr12: 27,368,635-91,765,744 , GRCh38.p12 chr12: 27,215,702-91,371,967 , ATP2B1, 1101 more genes
    nsv3924723copy number variation1nstd102humanPathogenic GRCh37 chr12: 70,163,517-77,357,997 , NCBI36 chr12: 68,449,784-75,882,128 , GRCh38 chr12: 69,769,737-76,964,217 KRR1, RNU4-65P, 80 more genes
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