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Items: 1 to 20 of 1726

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2678953copy number variation99estd199human GRCh37 chr18: 74,504,532-74,504,946 , GRCh38.p12 chr18: 76,792,576-76,792,990 ZNF236-DT
    esv2678936copy number variation165estd199human GRCh37 chr11: 34,249,375-34,249,700 , GRCh38.p12 chr11: 34,227,828-34,228,153 ABTB2
    esv2678926copy number variation224estd199human GRCh37 chr11: 20,569,190-20,571,247 , GRCh38.p12 chr11: 20,547,644-20,549,701 0
    esv2678974copy number variation795estd199human GRCh37 chr4: 7,524,423-7,524,667 , GRCh38.p12 chr4: 7,522,696-7,522,940 SORCS2
    esv2678946copy number variation74estd199human GRCh37 chr3: 50,443,369-50,444,820 , GRCh38.p12 chr3: 50,405,938-50,407,389 CACNA2D2
    esv2678845copy number variation733estd199human GRCh37 chr20: 11,517,265-11,517,588 , GRCh38.p12 chr20: 11,536,617-11,536,940 0
    esv2678873copy number variation195estd199human GRCh37 chr15: 89,868,207-89,868,576 , GRCh38.p12 chr15: 89,324,976-89,325,345 MIR6766, POLG
    esv2678844copy number variation315estd199human GRCh37 chr10: 33,492,640-33,492,929 , GRCh38.p12 chr10: 33,203,712-33,204,001 NRP1
    esv2678838copy number variation299estd199human GRCh37 chrX: 1,387,103-1,387,438 , GRCh38.p12 chrX: 1,268,210-1,268,545 CSF2RA
    esv2678803copy number variation613estd199human GRCh37 chr15: 34,200,447-34,200,714 , GRCh38.p12 chr15: 33,908,246-33,908,513 AVEN
    esv2678780copy number variation578estd199human GRCh37 chr13: 72,843,037-72,846,924 , GRCh38.p12 chr13: 72,268,899-72,272,786 0
    esv2678785copy number variation140estd199human GRCh37 chr12: 128,567,945-128,570,792 , GRCh38.p12 chr12: 128,083,400-128,086,247 LINC02369
    esv2678791copy number variation417estd199human GRCh37 chr11: 16,587,162-16,587,299 , GRCh38.p12 chr11: 16,565,615-16,565,752 SOX6
    esv2678781copy number variation25estd199human GRCh37 chr8: 120,926,325-120,926,719 , GRCh38.p12 chr8: 119,914,085-119,914,479 DEPTOR
    esv2678752copy number variation480estd199human GRCh37 chr7: 30,897,063-30,897,362 , GRCh38.p12 chr7: 30,857,447-30,857,746 MINDY4, INMT-MINDY4
    esv2678730copy number variation148estd199human GRCh37 chr6: 96,387,601-96,389,421 , GRCh38.p12 chr6: 95,939,725-95,941,545 LOC107986626
    esv2678723copy number variation70estd199human GRCh37 chr12: 2,017,891-2,018,055 , GRCh38.p12 chr12: 1,908,725-1,908,889 , GRCh38.p12 chr12|NW_018654718.1: 250,869-251,033 CACNA2D4
    esv2678692copy number variation34estd199human GRCh37 chr17: 15,183,458-15,185,695 , GRCh38.p12 chr17: 15,280,141-15,282,378 0
    esv2678595copy number variation23estd199human GRCh37 chr12: 80,823,356-80,828,244 , GRCh38.p12 chr12: 80,429,576-80,434,464 PTPRQ
    esv2678582copy number variation136estd199human GRCh37 chr12: 30,310,711-30,311,040 , GRCh38.p12 chr12: 30,157,778-30,158,107 0
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