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Items: 1 to 20 of 121

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076847inversion1nstd229human GRCh38 chr12: 120,561,098-121,398,093 , GRCh37.p13 chr12: 120,998,901-121,761,800 MIR4700, P2RX4, 27 more genes
    nsv6937005copy number variation1nstd229human GRCh38 chr12: 120,465,601-120,774,200 , GRCh37.p13 chr12: 120,903,404-121,212,003 DYNLL1, RNF10, 14 more genes
    nsv6935163copy number variation1nstd229human GRCh38 chr12: 120,067,201-120,694,800 , GRCh37.p13 chr12: 120,505,005-121,132,603 RPL11P5, RNF10, 30 more genes
    nsv6934866copy number variation1nstd229human GRCh38 chr12: 119,918,701-123,974,100 , GRCh37.p13 chr12: 120,356,505-124,458,647 RNU6-1088P, LOC105370042, 130 more genes
    nsv6934467copy number variation1nstd229human GRCh38 chr12: 120,407,101-120,775,400 , GRCh37.p13 chr12: 120,844,904-121,213,203 SPPL3, RPL31P52, 18 more genes
    nsv6930083copy number variation1nstd229human GRCh38 chr12: 120,251,001-120,606,400 , GRCh37.p13 chr12: 120,688,804-121,044,203 COX6A1, NRAV, 19 more genes
    nsv6919599copy number variation1nstd229human GRCh38 chr12: 119,989,801-120,740,500 , GRCh37.p13 chr12: 120,427,605-121,178,303 RPS20P31, MLEC, 33 more genes
    nsv6918781copy number variation1nstd229human GRCh38 chr12: 120,566,913-120,578,113 , GRCh37.p13 chr12: 121,004,716-121,015,916 RNF10, POP5
    nsv6637490copy number variation1nstd102humanUncertain significance GRCh37 chr12: 120,761,046-121,280,839 , GRCh38.p12 chr12: 120,323,243-120,843,036 RPS27P25, MIR4700, 22 more genes
    nsv6583876inversion1nstd223human GRCh38 chr12: 118,054,469-123,705,974 , GRCh37.p13 chr12: 118,492,274-124,190,521 RPL11P5, RPL17P37, 159 more genes
    nsv6495504copy number variation1nstd223human GRCh38 chr12: 120,566,913-120,578,109 , GRCh37.p13 chr12: 121,004,716-121,015,912 RNF10, POP5
    nsv6476788copy number variation1nstd223human GRCh38 chr12: 120,442,140-121,624,181 , GRCh37.p13 chr12: 120,879,943-121,761,800 RNU6-1004P, LOC105370030, 39 more genes
    nsv6290239copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 117,461,902-133,841,395 , GRCh38.p12 chr12: 117,024,097-133,264,809 ACADS, BCL7A, 356 more genes
    nsv6132412copy number variation1nstd213human GRCh37 chr12: 121,000,000-121,550,001 , GRCh38.p12 chr12: 120,562,197-121,112,198 ACADS, HNF1A, 21 more genes
    nsv5973346inversion1nstd209human GRCh38 chr12: 118,054,601-123,705,841 , GRCh37.p13 chr12: 118,492,406-124,190,388 , ACADS, 162 more genes
    nsv5555463sequence alteration1nstd206human GRCh38 chr12: 120,561,097-121,398,447 , GRCh37.p13 chr12: 120,998,900-121,761,800 P2RX7, OASL, 27 more genes
    nsv5265779copy number variation1nstd204human GRCh38.p13 chr12: 120,555,601-120,581,000 , GRCh37.p13 chr12: 120,993,404-121,018,803 POP5, RNF10
    nsv4756208inversion1nstd199human GRCh37 chr12: 104,359,633-125,801,147 , GRCh38.p12 chr12: 103,965,855-125,316,601 , ACACB, 453 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4754840inversion1nstd199human GRCh37 chr12: 104,382,539-125,801,164 , GRCh38.p12 chr12: 103,988,761-125,316,618 , ACACB, 452 more genes
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