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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5470787copy number variation1nstd206human GRCh38 chr6: 106,112,750-106,457,587 , GRCh37.p13 chr6: 106,560,625-106,905,462 CRYBG1, ATG5, 4 more genes
    nsv5381620copy number variation1nstd102humanUncertain significance GRCh37 chr6: 106,756,239-107,365,536 , GRCh38.p12 chr6: 106,308,364-107,044,332 CRYBG1, RPL21P65, 17 more genes
    nsv5102971mobile element insertion1nstd203human GRCh38 chr6: 106,455,490-106,455,506 , GRCh37.p13 chr6: 106,903,365-106,903,381 LOC105377924, CRYBG1
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4945510copy number variation1nstd200human GRCh38 chr6: 106,452,802-106,511,647 , GRCh37.p13 chr6: 106,900,677-106,959,522 CRYBG1, LOC101927405, 1 more genes
    nsv4824598copy number variation1nstd200human GRCh37 chr6: 106,900,677-106,959,522 , GRCh38.p12 chr6: 106,452,802-106,511,647 CRYBG1, LOC101927405, 1 more genes
    nsv4768376copy number variation1nstd102humanPathogenic GRCh37 chr6: 98,949,950-114,533,905 , GRCh38.p12 chr6: 98,502,074-114,212,741 LOC101927405, GPR6, 211 more genes
    nsv4685989copy number variation1nstd102humanPathogenic GRCh37 chr6: 101,287,058-117,013,245 , GRCh38.p12 chr6: 100,839,182-116,692,082 RPL23AP50, RNU6-960P, 216 more genes
    nsv4675798copy number variation1nstd102humanLikely benign GRCh37 chr6: 106,814,261-107,222,454 , GRCh38.p12 chr6: 106,366,386-106,774,579 LINC02526, QRSL1, 10 more genes
    nsv4675563copy number variation1nstd102humanUncertain significance GRCh37 chr6: 106,638,006-107,421,916 , GRCh38.p12 chr6: 106,190,131-107,100,712 QRSL1, ATG5, 20 more genes
    nsv4480469mobile element insertion1nstd166human GRCh37.p13 chr6: 106,901,487-106,901,487 , GRCh38.p12 chr6: 106,453,612-106,453,612 CRYBG1, LOC105377924
    nsv4455536copy number variation1nstd102humanUncertain significance GRCh37 chr6: 106,877,325-107,082,724 , GRCh38.p12 chr6: 106,429,450-106,634,849 CRYBG1, RTN4IP1, 5 more genes
    nsv4398726copy number variation1nstd174human GRCh37 chr6: 106,529,777-106,912,047 , GRCh38.p12 chr6: 106,081,902-106,464,172 CRYBG1, PRDM1, 5 more genes
    nsv4387888copy number variation2nstd173human GRCh37 chr6: 106,851,288-106,903,900 , GRCh38.p12 chr6: 106,403,413-106,456,025 RNA5SP211, CRYBG1, 1 more genes
    nsv4338438sequence alteration1nstd166human GRCh38.p12 chr6: 105,915,838-106,522,778 , GRCh37.p13 chr6: 106,363,713-106,970,653 CRYBG1, PRDM1, 6 more genes
    nsv4330897inversion1nstd166human GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351 , ACAT2, 894 more genes
    nsv4312499inversion1nstd166human GRCh37.p13 chr6: 94,532,001-117,422,619 , GRCh38.p12 chr6: 93,822,283-117,101,456 , CRYBG1, 284 more genes
    nsv3960618insertion1nstd168human GRCh38 chr6: 106,438,479-106,491,557 , GRCh37.p13 chr6: 106,886,354-106,939,432 CRYBG1, RNA5SP211, 2 more genes
    nsv3924576copy number variation1nstd102humanPathogenic NCBI36 chr6: 97,164,591-122,524,393 , GRCh38 chr6: 96,609,994-122,161,548 , GRCh37 chr6: 97,057,870-122,482,694 TUBE1, PLN, 318 more genes
    nsv3919897copy number variation1nstd102humanPathogenic NCBI36 chr6: 103,834,033-114,362,096 , GRCh37 chr6: 103,727,340-114,255,403 , GRCh38 chr6: 103,279,465-113,934,239 HACE1, RNU6-1144P, 174 more genes
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