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Items: 1 to 20 of 192

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146279insertion1nstd232human GRCh37.p13 chr3: 53,265,569-53,265,569 , GRCh38.p12 chr3: 53,231,553-53,231,553 TKT
    nsv7143883copy number variation1nstd232human GRCh37.p13 chr3: 53,263,152-53,263,293 , GRCh38.p12 chr3: 53,229,136-53,229,277 TKT
    nsv7138534insertion1nstd232human GRCh37.p13 chr3: 53,260,894-53,260,894 , GRCh38.p12 chr3: 53,226,878-53,226,878 TKT
    nsv7138317insertion1nstd232human GRCh37.p13 chr3: 53,269,957-53,269,957 , GRCh38.p12 chr3: 53,235,941-53,235,941 TKT
    nsv7137788insertion1nstd232human GRCh37.p13 chr3: 53,263,453-53,263,453 , GRCh38.p12 chr3: 53,229,437-53,229,437 TKT
    nsv7096813copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,018,081-53,845,433 , GRCh38.p12 chr3: 51,984,065-53,811,406 DNAH1, BAP1, 62 more genes
    nsv6717609copy number variation1nstd229human GRCh38 chr3: 53,113,856-53,320,010 , GRCh37.p13 chr3: 53,185,062-53,354,037 , GRCh37.p13 chr3|NW_004775426.1: 1-168,965 LOC107986087, RFT1, 3 more genes
    nsv6712502copy number variation1nstd229human GRCh38 chr3: 52,907,701-53,526,800 , GRCh37.p13 chr3: 52,941,717-53,560,827 SNORD38C, LOC107986087, 9 more genes
    nsv6711857copy number variation1nstd229human GRCh38 chr3: 53,225,359-53,225,546 , GRCh37.p13 chr3|NW_004775426.1: 74,314-74,501 , GRCh37.p13 chr3: 53,259,375-53,259,562 TKT
    nsv6705610copy number variation1nstd229human GRCh38 chr3: 53,228,893-53,228,950 , GRCh37.p13 chr3: 53,262,909-53,262,966 , GRCh37.p13 chr3|NW_004775426.1: 77,848-77,905 TKT
    nsv6699724copy number variation1nstd229human GRCh38 chr3: 53,256,182-53,262,035 , GRCh37.p13 chr3: 53,290,198-53,296,051 , GRCh37.p13 chr3|NW_004775426.1: 105,137-110,990 TKT
    nsv6699023copy number variation1nstd229human GRCh38 chr3: 52,811,798-54,282,378 , GRCh37.p13 chr3: 52,845,814-54,316,405 LOC105377095, SERBP1P3, 22 more genes
    nsv6636925copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,780,509-53,418,869 , GRCh38.p12 chr3: 52,746,493-53,384,842 LOC105377094, ITIH4-AS1, 17 more genes
    nsv6636758copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,783,975-53,418,893 , GRCh38.p12 chr3: 52,749,959-53,384,866 NEK4, MUSTN1, 17 more genes
    nsv6541068inversion1nstd223human GRCh38 chr3: 53,248,529-53,249,103 , GRCh37.p13 chr3: 53,282,545-53,283,119 , GRCh37.p13 chr3|NW_004775426.1: 97,484-98,058 TKT
    nsv6369827copy number variation1nstd223human GRCh38 chr3: 52,164,358-54,467,618 , GRCh37.p13 chr3: 52,198,374-54,501,645 SEMA3G, STAB1, 61 more genes
    nsv6367735copy number variation1nstd223human GRCh38 chr3: 52,941,201-53,367,100 , GRCh37.p13 chr3|NW_004775426.1: 1-216,055 , GRCh37.p13 chr3: 53,185,062-53,401,127 TKT, DCP1A, 7 more genes
    nsv6362677copy number variation1nstd223human GRCh38 chr3: 53,256,177-53,262,029 , GRCh37.p13 chr3|NW_004775426.1: 105,132-110,984 , GRCh37.p13 chr3: 53,290,193-53,296,045 TKT
    nsv6358096copy number variation1nstd223human GRCh38 chr3: 53,242,743-53,243,384 , GRCh37.p13 chr3: 53,276,759-53,277,400 , GRCh37.p13 chr3|NW_004775426.1: 91,698-92,339 TKT
    nsv6357735copy number variation1nstd223human GRCh38 chr3: 53,237,744-53,242,384 , GRCh37.p13 chr3|NW_004775426.1: 86,699-91,339 , GRCh37.p13 chr3: 53,271,760-53,276,400 TKT
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