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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3921061copy number variation1nstd102humanBenign/Likely benign GRCh37 chr13: 92,173,306-92,249,821 , NCBI36 chr13: 90,971,307-91,047,822 , GRCh38 chr13: 91,521,052-91,597,567 GPC5
    nsv3922208copy number variation1nstd102humanBenign/Likely benign GRCh38 chr8: 16,094,502-16,164,176 , NCBI36 chr8: 15,996,382-16,066,056 , GRCh37 chr8: 15,952,011-16,021,685 MSR1
    nsv3895487copy number variation1nstd102humanBenign/Likely benign GRCh38 chr3: 2,475,307-2,540,154 , GRCh37 chr3: 2,516,991-2,581,838 , NCBI36 chr3: 2,491,991-2,556,838 CNTN4
    nsv3916025copy number variation3nstd102humanBenign/Likely benign, Likely benign GRCh38 chr6: 57,052,810-57,085,760 , GRCh37 chr6: 56,917,608-56,950,558 KIAA1586
    nsv3894794copy number variation1nstd102humanBenign/Likely benign GRCh37 chr7: 142,829,167-142,836,798 , GRCh38.p12 chr7: 143,132,074-143,139,705 PIP
    nsv3917152copy number variation1nstd102humanBenign/Likely benign GRCh37 chr7: 100,980,697-101,126,335 , NCBI36 chr7: 100,767,417-100,913,055 , GRCh38 chr7: 101,337,416-101,483,054 COL26A1
    nsv3887282copy number variation2nstd102humanBenign/Likely benign GRCh37 chrX: 101,596,705-101,693,437 , GRCh38.p12 chrX: 102,341,782-102,438,516 NXF2B
    nsv3922421copy number variation1nstd102humanBenign/Likely benign GRCh38 chr17: 47,522,632-47,585,157 , GRCh37 chr17: 45,599,998-45,662,523 , NCBI36 chr17: 42,954,997-43,017,522 NPEPPS
    nsv3914128copy number variation1nstd102humanBenign/Likely benign GRCh37 chr7: 79,337,679-79,393,170 , NCBI36 chr7: 79,175,615-79,231,106 , GRCh38 chr7: 79,708,363-79,763,854 LOC105375370
    nsv3913744copy number variation1nstd102humanBenign/Likely benign GRCh38 chr3: 119,033,541-119,081,373 , GRCh37 chr3: 118,752,388-118,800,220 , NCBI36 chr3: 120,235,078-120,282,910 IGSF11
    nsv3911314copy number variation1nstd102humanBenign/Likely benign NCBI36 chr20: 8,734-56,266 , GRCh38 chr20: 80,093-127,625 , GRCh37 chr20: 60,734-108,266 DEFB125
    nsv3923673copy number variation1nstd102humanBenign/Likely benign GRCh37 chr5: 71,913-116,846 , NCBI36 chr5: 124,913-169,846 , GRCh38 chr5: 71,798-116,731 PLEKHG4B
    nsv3917146copy number variation1nstd102humanBenign/Likely benign GRCh37 chr8: 73,596,927-73,635,634 , GRCh38 chr8: 72,684,692-72,723,399 , NCBI36 chr8: 73,759,481-73,798,188 KCNB2
    nsv3890190copy number variation1nstd102humanBenign/Likely benign GRCh37 chr12: 148,034-176,816 , GRCh38.p12 chr12|NW_003571049.1: 33,495-61,665 , GRCh38.p12 chr12: 45,740-67,650 IQSEC3
    nsv3916632copy number variation1nstd102humanBenign/Likely benign GRCh38 chr22: 16,786,503-16,809,385 , GRCh37 chr22: 17,267,393-17,290,275 , NCBI36 chr22: 15,647,393-15,670,275 XKR3
    nsv3921091copy number variation1nstd102humanBenign/Likely benign GRCh37 chr3: 118,778,681-118,800,220 , NCBI36 chr3: 120,261,371-120,282,910 , GRCh38 chr3: 119,059,834-119,081,373 IGSF11
    nsv3871234copy number variation1nstd102humanBenign/Likely benign GRCh37 chr2: 241,556,949-241,578,483 , GRCh38.p12 chr2: 240,617,532-240,639,066 GPR35
    nsv3892428copy number variation1nstd102humanBenign/Likely benign GRCh37 chr7: 42,226,378-42,244,825 , GRCh38.p12 chr7: 42,186,779-42,205,226 GLI3
    nsv3894347copy number variation1nstd102humanBenign/Likely benign GRCh37 chr16: 86,519,903-86,536,742 , GRCh38.p12 chr16: 86,486,297-86,503,136 FENDRR
    nsv3902711copy number variation1nstd102humanBenign/Likely benign GRCh37 chr10: 49,367,155-49,382,926 , GRCh38.p12 chr10: 48,159,112-48,174,883 FRMPD2
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