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Items: 1 to 20 of 147

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148229copy number variation1nstd102humanPathogenic GRCh38 chr4: 2,904,667-42,963,232 , GRCh37.p13 chr4: 2,906,394-42,965,249 LINC01587, RN7SKP82, 509 more genes
    nsv7148161copy number variation1nstd102humanPathogenic GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194 SLIRPP2, STIM2-AS1, 659 more genes
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7137196copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-34,512,694 , GRCh38.p12 chr4: 68,453-34,511,072 ECM1P2, LOC105378240, 482 more genes
    nsv7098818copy number variation1nstd102humanPathogenic GRCh38 chr4: 11,399,082-38,137,335 , GRCh37.p13 chr4: 11,400,706-38,138,956 LOC105374542, PPARGC1A, 232 more genes
    nsv7047237inversion1nstd229human GRCh38 chr4: 15,975,453-25,472,708 , GRCh37.p13 chr4: 15,977,076-25,474,330 LOC107986219, LOC102723675, 78 more genes
    nsv7041180inversion1nstd229human GRCh38 chr4: 18,154,007-23,460,918 , GRCh37.p13 chr4: 18,155,630-23,462,541 RPL21P46, LOC105374511, 28 more genes
    nsv6727983copy number variation1nstd229human GRCh38 chr4: 21,846,663-21,847,046 , GRCh37.p13 chr4: 21,848,286-21,848,669 KCNIP4, KCNIP4-IT1
    nsv6726429copy number variation1nstd229human GRCh38 chr4: 21,836,771-21,842,307 , GRCh37.p13 chr4: 21,838,394-21,843,930 KCNIP4-IT1, KCNIP4
    nsv6637075copy number variation1nstd102humanUncertain significance GRCh37 chr4: 16,249,194-24,864,955 , GRCh38.p12 chr4: 16,247,571-24,863,333 LOC107986262, QDPR, 63 more genes
    nsv6634358copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LINC02475, LOC105374344, 658 more genes
    nsv6629612copy number variation1nstd224human GRCh37 chr4: 21,718,241-21,866,369 , GRCh38.p12 chr4: 21,716,618-21,864,746 KCNIP4-IT1, KCNIP4
    nsv6367386copy number variation1nstd223human GRCh38 chr4: 21,841,381-21,842,042 , GRCh37.p13 chr4: 21,843,004-21,843,665 KCNIP4, KCNIP4-IT1
    nsv6362618copy number variation1nstd223human GRCh38 chr4: 21,842,201-21,843,300 , GRCh37.p13 chr4: 21,843,824-21,844,923 KCNIP4-IT1, KCNIP4
    nsv6362254copy number variation1nstd223human GRCh38 chr4: 17,003,809-24,506,634 , GRCh37.p13 chr4: 17,005,432-24,508,257 CLRN2, LOC107986220, 48 more genes
    nsv6361106copy number variation1nstd223human GRCh38 chr4: 21,843,801-21,845,800 , GRCh37.p13 chr4: 21,845,424-21,847,423 KCNIP4-IT1, KCNIP4
    nsv6315440copy number variation1nstd102humanPathogenic GRCh37 chr4: 114,784-47,569,569 , GRCh38.p12 chr4: 114,902-47,567,552 FAM86KP, ENPP7P11, 631 more genes
    nsv6313814copy number variation1nstd102humanUncertain significance GRCh37 chr4: 21,086,170-22,598,608 , GRCh38.p12 chr4: 21,084,547-22,596,985 MIR7978, KCNIP4-IT1, 8 more genes
    nsv6313559copy number variation1nstd102humanPathogenic GRCh37 chr4: 19,892,850-37,325,128 , GRCh38.p12 chr4: 19,891,227-37,323,506 LOC102723846, KCNIP4-IT1, 135 more genes
    nsv6135326copy number variation1nstd213human GRCh37 chr4: 21,690,000-22,170,001 , GRCh38.p12 chr4: 21,688,377-22,168,378 KCNIP4, KCNIP4-IT1, 1 more genes
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