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Items: 1 to 20 of 568

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147034copy number variation1nstd232human GRCh37.p13 chr8: 145,622,628-145,622,700 , GRCh38.p12 chr8: 144,397,413-144,397,485 , GRCh38.p12 chr8|NW_018654716.1: 128,016-128,088 CPSF1
    nsv7146833insertion1nstd232human GRCh37.p13 chr8: 145,537,320-145,537,320 , GRCh38.p12 chr8: 144,313,634-144,313,634 , GRCh38.p12 chr8|NW_018654716.1: 44,237-44,237 HSF1, DGAT1
    nsv7146018copy number variation1nstd232human GRCh37.p13 chr8: 145,505,306-145,505,365 , GRCh38.p12 chr8: 144,281,543-144,281,602 , GRCh38.p12 chr8|NW_018654716.1: 12,146-12,205 BOP1
    nsv7144017copy number variation1nstd232human GRCh38.p12 chr8: 144,393,365-144,393,450 , GRCh37.p13 chr8: 145,618,580-145,618,665 , GRCh38.p12 chr8|NW_018654716.1: 123,968-124,053 CPSF1, ADCK5, 1 more genes
    nsv7143180copy number variation1nstd232human GRCh37.p13 chr8: 145,535,286-145,535,383 , GRCh38.p12 chr8|NW_018654716.1: 42,203-42,300 , GRCh38.p12 chr8: 144,311,600-144,311,697 HSF1
    nsv7142277copy number variation1nstd232human GRCh37.p13 chr8: 145,503,113-145,503,194 , GRCh38.p12 chr8: 144,279,080-144,279,161 , GRCh38.p12 chr8|NW_018654716.1: 9,683-9,764 BOP1
    nsv7141611insertion1nstd232human GRCh37.p13 chr8: 145,579,954-145,579,954 , GRCh38.p12 chr8: 144,356,294-144,356,294 , GRCh38.p12 chr8|NW_018654716.1: 86,897-86,897 FBXL6
    nsv7140940copy number variation1nstd232human GRCh38.p12 chr8: 144,400,084-144,400,163 , GRCh37.p13 chr8: 145,625,474-145,625,557 , GRCh38.p12 chr8|NW_018654716.1: 130,687-130,766 CPSF1, MIR1234, 1 more genes
    nsv7139729copy number variation1nstd232human GRCh37.p13 chr8: 145,606,844-145,607,055 , GRCh38.p12 chr8: 144,381,643-144,381,854 , GRCh38.p12 chr8|NW_018654716.1: 112,246-112,457 ADCK5
    nsv7139475copy number variation1nstd232human GRCh37.p13 chr8: 145,510,190-145,510,254 , GRCh38.p12 chr8: 144,286,489-144,286,553 , GRCh38.p12 chr8|NW_018654716.1: 17,092-17,156 BOP1
    nsv7138265copy number variation1nstd232human GRCh37.p13 chr8: 145,573,306-145,573,372 , GRCh38.p12 chr8: 144,349,641-144,349,707 , GRCh38.p12 chr8|NW_018654716.1: 80,244-80,310 0
    nsv7097898copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,654,526-145,656,554 , GRCh38.p12 chr8: 144,429,143-144,431,171 , GRCh38.p12 chr8|NW_018654716.1: 159,745-161,773 TONSL
    nsv7097897copy number variation1nstd102humanPathogenic GRCh37 chr8: 145,639,206-145,643,123 , GRCh38.p12 chr8: 144,413,822-144,417,739 , GRCh38.p12 chr8|NW_018654716.1: 144,425-148,342 SLC39A4
    nsv7097896copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,582,954-145,584,675 , GRCh38.p12 chr8: 144,359,294-144,361,015 , GRCh38.p12 chr8|NW_018654716.1: 89,897-91,618 SLC52A2
    nsv7097654copy number variation1nstd102humanPathogenic GRCh37 chr8: 145,637,954-145,644,386 , GRCh38.p12 chr8|NW_018654716.1: 143,173-149,605 , GRCh38.p12 chr8: 144,412,570-144,419,002 SLC39A4
    nsv7097653copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,584,230-145,584,675 , GRCh38.p12 chr8|NW_018654716.1: 91,173-91,618 , GRCh38.p12 chr8: 144,360,570-144,361,015 SLC52A2
    nsv6635631copy number variation1nstd227human GRCh38.p12 chr8: 144,351,265-144,509,999 , GRCh37 chr8: 145,574,930-145,735,382 , GRCh38.p12 chr8|NW_018654716.1: 81,868-165,120 GPT, TONSL, 21 more genes
    nsv6634880copy number variation1nstd227human GRCh38.p12 chr8: 144,351,265-144,515,746 , GRCh37 chr8: 145,574,930-145,741,130 , GRCh38.p12 chr8|NW_018654716.1: 81,868-165,120 GPT, TONSL, 21 more genes
    nsv6312628copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 145,658,472-145,660,261 , GRCh38.p12 chr8: 144,433,089-144,434,878 , GRCh38.p12 chr8|NW_018654716.1: 163,691-165,120 TONSL, TONSL-AS1, 1 more genes
    nsv6312627copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,540,217-145,550,299 , GRCh38.p12 chr8|NW_018654716.1: 47,157-57,239 , GRCh38.p12 chr8: 144,316,554-144,326,636 MIR6848, DGAT1
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