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Items: 1 to 20 of 157

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5681854mobile element insertion1nstd211human GRCh38 chr6: 85,459,998-85,459,998 , GRCh37.p13 chr6: 86,169,716-86,169,716 NT5E
    nsv5401734mobile element insertion1nstd206human GRCh38 chr6: 85,459,998-85,460,040 , GRCh37.p13 chr6: 86,169,716-86,169,758 NT5E
    nsv5378582translocation1nstd200human GRCh38 chr6: 85,474,404-85,474,404 , GRCh38 chr6: 85,477,190-85,477,190 , GRCh37.p13 chr6: 86,186,908-86,186,908 , GRCh37.p13 chr6: 86,184,122-86,184,122 NT5E
    nsv5378581translocation1nstd200human GRCh38 chr6: 85,474,380-85,474,380 , GRCh38 chr6: 85,476,134-85,476,134 , GRCh37.p13 chr6: 86,184,098-86,184,098 , GRCh37.p13 chr6: 86,185,852-86,185,852 NT5E
    nsv5119362mobile element insertion1nstd203human GRCh38 chr6: 85,486,794-85,486,805 , GRCh37.p13 chr6: 86,196,512-86,196,523 NT5E
    nsv5108097mobile element insertion1nstd203human GRCh38 chr6: 85,463,246-85,463,262 , GRCh37.p13 chr6: 86,172,964-86,172,980 NT5E
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv5037999inversion1nstd200human GRCh38 chr6: 85,122,647-85,919,417 , GRCh37.p13 chr6: 85,832,365-86,629,135 , LOC100127917, 19 more genes
    nsv4945368copy number variation1nstd200human GRCh38 chr6: 84,932,542-85,530,791 , GRCh37.p13 chr6: 85,642,260-86,240,509 LOC105377881, NT5E, 9 more genes
    nsv4941927copy number variation1nstd200human GRCh38 chr6: 85,446,087-85,449,526 , GRCh37.p13 chr6: 86,155,805-86,159,244 NT5E
    nsv4878533inversion1nstd200human GRCh37 chr6: 85,832,365-86,629,135 , GRCh38.p12 chr6: 85,122,647-85,919,417 , SNX14, 19 more genes
    nsv4685712copy number variation1nstd102humanUncertain significance GRCh37 chr6: 85,832,618-86,578,811 , GRCh38.p12 chr6: 85,122,900-85,869,093 PKMP3, LINC02535, 17 more genes
    nsv4675039copy number variation1nstd102humanPathogenic GRCh37 chr6: 86,024,761-90,023,713 , GRCh38.p12 chr6: 85,315,043-89,313,994 C6orf163, LOC100652960, 65 more genes
    nsv4456953copy number variation1nstd102humanUncertain significance GRCh37 chr6: 86,155,642-86,252,892 , GRCh38.p12 chr6: 85,445,924-85,543,174 NT5E, SNX14
    nsv4373934copy number variation1nstd173human GRCh37 chr6: 86,175,673-86,264,355 , GRCh38.p12 chr6: 85,465,955-85,554,637 NT5E, SNX14
    nsv4139209copy number variation1nstd166human GRCh37.p13 chr6: 86,175,024-86,176,128 , GRCh38.p12 chr6: 85,465,306-85,466,410 NT5E
    nsv3923528copy number variation1nstd102humanPathogenic NCBI36 chr6: 84,604,741-99,376,910 , GRCh38 chr6: 83,838,303-98,822,313 , GRCh37 chr6: 84,548,022-99,270,189 RNU4-72P, LOC100132830, 157 more genes
    nsv3922883copy number variation1nstd102humanPathogenic NCBI36 chr6: 85,811,199-89,199,075 , GRCh37.p13 chr6: 85,754,480-89,142,356 , GRCh38.p12 chr6: 85,044,762-88,432,637 RN7SL643P, RPL7P27, 57 more genes
    nsv3921478copy number variation1nstd102humanPathogenic NCBI36 chr6: 76,692,636-93,477,232 , GRCh38 chr6: 75,926,199-92,710,793 , GRCh37 chr6: 76,635,916-93,420,511 SPACA1, TAF13P1, 187 more genes
    nsv3919111copy number variation1nstd102humanPathogenic GRCh38 chr6: 74,382,807-142,040,500 , NCBI36 chr6: 75,149,243-142,403,330 , GRCh37 chr6: 75,092,523-142,361,637 RNU6-770P, MAP3K5-AS2, 810 more genes
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