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Items: 1 to 20 of 26

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3923759copy number variation1nstd102humanPathogenic NCBI36 chr4: 58,862,002-102,129,682 , GRCh37.p13 chr4: 59,167,245-101,910,659 , GRCh38.p12 chr4: 58,301,079-100,989,502 PIGY, EREG, 530 more genes
    nsv3923733copy number variation1nstd102humanPathogenic GRCh38 chr4: 80,427,023-100,855,441 , GRCh37 chr4: 81,348,177-101,776,598 , NCBI36 chr4: 81,567,201-101,995,621 PIGY, PDLIM5, 215 more genes
    nsv7148241copy number variation1nstd102humanPathogenic GRCh38 chr4: 79,123,548-99,457,773 , GRCh37.p13 chr4: 80,044,702-100,378,930 PIGY, LOC105377327, 214 more genes
    nsv3888958copy number variation1nstd102humanPathogenic GRCh37 chr4: 81,314,915-96,636,651 , GRCh38.p12 chr4: 80,393,761-95,715,500 PIGY, LOC391674, 156 more genes
    nsv6313484copy number variation1nstd102humanPathogenic GRCh37 chr4: 79,780,152-94,873,225 , GRCh38.p12 chr4: 78,858,998-93,952,074 PIGY, LOC105377329, 166 more genes
    nsv3912429copy number variation1nstd102humanPathogenic GRCh37 chr4: 81,800,931-95,730,598 , NCBI36 chr4: 82,019,955-95,949,621 , GRCh38 chr4: 80,879,777-94,809,447 PIGY, RNU6-469P, 152 more genes
    nsv6291249copy number variation1nstd102humanPathogenic GRCh37 chr4: 80,467,886-93,362,064 , GRCh38.p12 chr4: 79,546,732-92,440,913 PIGY, HNRNPA3P13, 155 more genes
    nsv3916835copy number variation1nstd102humanPathogenic GRCh37 chr4: 80,496,902-93,333,600 , GRCh38 chr4: 79,575,748-92,412,449 , NCBI36 chr4: 80,715,926-93,552,623 PIGY, SLC10A6, 155 more genes
    nsv4436731copy number variation1nstd102humanPathogenic GRCh37 chr4: 80,482,400-92,572,499 , GRCh38.p12 chr4: 79,561,246-91,651,348 PIGY, HERC5, 150 more genes
    nsv6313848copy number variation1nstd102humanPathogenic GRCh37 chr4: 81,054,789-90,667,421 , GRCh38.p12 chr4: 80,133,635-89,746,270 PIGY, RPL6P13, 136 more genes
    nsv3915919copy number variation1nstd102humanPathogenic NCBI36 chr4: 85,469,728-94,794,648 , GRCh37.p13 chr4: 85,250,704-94,575,625 , GRCh38.p12 chr4: 84,329,551-93,654,474 PIGY, RNU6-907P, 89 more genes
    nsv3910328copy number variation1nstd102humanPathogenic GRCh37 chr4: 86,370,518-94,894,345 , GRCh38 chr4: 85,449,365-93,973,194 , NCBI36 chr4: 86,589,542-95,113,368 PIGY, LOC112268468, 81 more genes
    nsv3875754copy number variation1nstd102humanPathogenic GRCh37 chr4: 82,283,358-90,341,831 , GRCh38.p12 chr4: 81,362,204-89,420,680 PIGY, LOC152845, 121 more genes
    nsv3883611copy number variation1nstd102humanPathogenic GRCh37 chr4: 85,839,771-93,071,150 , GRCh38.p12 chr4: 84,918,618-92,149,999 PIGY, HERC5, 78 more genes
    nsv3920373copy number variation1nstd102humanPathogenic NCBI36 chr4: 88,484,512-94,794,609 , GRCh37.p13 chr4: 88,265,488-94,575,586 , GRCh38.p12 chr4: 87,344,336-93,654,435 PIGY, RN7SKP244, 58 more genes
    nsv4685891copy number variation1nstd102humanPathogenic GRCh37 chr4: 88,075,149-90,714,489 , GRCh38.p12 chr4: 87,153,997-89,793,338 PIGY, LOC100419572, 50 more genes
    nsv3873978copy number variation1nstd102humanPathogenic GRCh37 chr4: 11,525-191,028,879 , GRCh38.p12 chr4: 11,525-190,107,724 PIGY, LOC100422029, 2358 more genes
    nsv3876533copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-190,963,766 , GRCh38.p12 chr4: 49,556-190,042,611 PIGY, LOC100420289, 2347 more genes
    nsv3884499copy number variation1nstd102humanPathogenic GRCh37 chr4: 12,440-190,904,441 , GRCh38.p12 chr4: 12,440-189,983,286 PIGY, MTND4LP29, 2341 more genes
    nsv3880085copy number variation2nstd102humanPathogenic GRCh37 chr4: 68,346-190,957,473 , GRCh38.p12 chr4: 68,454-190,036,318 PIGY, LOC112268460, 2345 more genes
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