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Items: 1 to 20 of 169

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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
    nsv6734580copy number variation1nstd229human GRCh38 chr4: 26,481,384-26,485,750 , GRCh37.p13 chr4: 26,483,006-26,487,372 CCKAR
    nsv6729207copy number variation1nstd229human GRCh38 chr4: 25,780,101-26,536,200 , GRCh37.p13 chr4: 25,781,723-26,537,822 LOC105374542, LOC105374545, 9 more genes
    nsv6726375copy number variation1nstd229human GRCh38 chr4: 26,476,441-26,483,582 , GRCh37.p13 chr4: 26,478,063-26,485,204 CCKAR
    nsv6725012copy number variation1nstd229human GRCh38 chr4: 26,431,201-26,492,700 , GRCh37.p13 chr4: 26,432,823-26,494,322 RBPJ, CCKAR
    nsv6634358copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LINC02475, LOC105374344, 658 more genes
    nsv6629477copy number variation1nstd224human GRCh37 chr4: 26,480,145-26,501,114 , GRCh38.p12 chr4: 26,478,523-26,499,492 CCKAR
    nsv6315440copy number variation1nstd102humanPathogenic GRCh37 chr4: 114,784-47,569,569 , GRCh38.p12 chr4: 114,902-47,567,552 FAM86KP, ENPP7P11, 631 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
    nsv6135075copy number variation1nstd213human GRCh37 chr4: 26,490,000-28,040,001 , GRCh38.p12 chr4: 26,488,378-28,038,379 CCKAR, TBC1D19, 12 more genes
    nsv6112761copy number variation1nstd102humanPathogenic GRCh37 chr4: 69,671-29,702,595 , GRCh38.p12 chr4: 69,779-29,700,973 LOC101928306, PDE6B-AS1, 460 more genes
    nsv6078560insertion1nstd212human GRCh38 chr4: 26,484,866-26,484,866 , GRCh37.p13 chr4: 26,486,488-26,486,488 CCKAR
    nsv5966364insertion1nstd209human GRCh38 chr4: 26,484,866-26,484,866 , GRCh37.p13 chr4: 26,486,488-26,486,488 CCKAR
    nsv5906067copy number variation1nstd209human GRCh38 chr4: 22,920,705-27,042,181 , GRCh37.p13 chr4: 22,922,328-27,043,803 , SEPSECS, 49 more genes
    nsv5623480insertion1nstd207human GRCh38 chr4: 26,484,866-26,484,866 , GRCh37.p13 chr4: 26,486,488-26,486,488 CCKAR
    nsv5555293inversion1nstd206human GRCh38 chr4: 26,484,974-26,485,833 , GRCh37.p13 chr4: 26,486,596-26,487,455 CCKAR
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