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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3960265copy number variation1nstd168human GRCh38 (hg38) chr5: 122,861,797-122,941,355 , GRCh37.p13 chr5: 122,197,492-122,277,050 SNX24
    nsv3939739copy number variation1nstd167human GRCh37 (hg19) chr5: 122,274,354-122,274,677 , GRCh38.p12 chr5: 122,938,659-122,938,982 SNX24
    nsv3924205copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr5: 110,687,442-130,103,838 , GRCh37.p13 chr5: 110,023,143-129,439,531 , NCBI36 (hg18) chr5: 110,051,042-129,467,430 SNX24, CSNK1G3, 230 more genes
    nsv3923804copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr5: 108,308,463-125,777,797 , GRCh37.p13 chr5: 107,644,164-125,113,490 , NCBI36 (hg18) chr5: 107,672,063-125,141,389 SNX24, CSNK1G3, 200 more genes
    nsv3923717copy number variation1nstd102humanUncertain significance GRCh38 (hg38) chr5: 122,479,268-126,833,168 , GRCh37.p13 chr5: 121,814,963-126,168,860 , NCBI36 (hg18) chr5: 121,842,862-126,196,759 SNX24, SNX2, 49 more genes
    nsv3921962copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr5: 114,707,561-126,507,744 , GRCh37.p13 chr5: 114,043,258-125,843,436 , NCBI36 (hg18) chr5: 114,071,157-125,871,335 SNX24, AP3S1, 136 more genes
    nsv3919087copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr5: 120,739,630-126,823,984 , GRCh37.p13 chr5: 120,075,325-126,159,676 , NCBI36 (hg18) chr5: 120,103,224-126,187,575 SNX24, LOX, 66 more genes
    nsv3916468copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr5: 90,374,606-128,076,423 , GRCh37.p13 chr5: 89,670,423-127,412,115 , NCBI36 (hg18) chr5: 89,706,179-127,440,014 SNX24, CAST, 415 more genes
    nsv3915450copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr5: 91,411,708-131,319,563 , GRCh37.p13 chr5: 90,707,525-130,655,256 , NCBI36 (hg18) chr5: 90,743,281-130,683,155 SNX24, ALDH7A1, 432 more genes
    nsv3912937copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr5: 106,619,588-156,124,387 , GRCh37.p13 chr5: 105,955,289-155,551,397 , NCBI36 (hg18) chr5: 105,983,188-155,483,975 SNX24, CAMK4, 795 more genes
    nsv3912909copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr5: 120,695,675-124,525,372 , GRCh37.p13 chr5: 120,031,370-123,861,065 , NCBI36 (hg18) chr5: 120,059,269-123,888,964 SNX24, CSNK1G3, 41 more genes
    nsv3912712copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr5: 116,677,122-132,686,163 , GRCh37.p13 chr5: 116,012,818-132,021,855 , NCBI36 (hg18) chr5: 116,040,717-132,049,754 SNX24, ACTBP4, 187 more genes
    nsv3912593copy number variation1nstd102humanUncertain significance NCBI36 (hg18) chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259 SNX24, ACTBP4, 2580 more genes
    nsv3911092copy number variation1nstd102humanUncertain significance GRCh38 (hg38) chr5: 118,854,384-122,849,602 , GRCh37.p13 chr5: 118,190,079-122,185,297 , NCBI36 (hg18) chr5: 118,217,978-122,213,196 SNX24, HSD17B4, 48 more genes
    nsv3910959copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr5: 111,463,016-127,193,038 , GRCh37.p13 chr5: 110,798,714-126,528,730 , NCBI36 (hg18) chr5: 110,826,613-126,556,629 SNX24, ALDH7A1, 191 more genes
    nsv3889848copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719 , NCBI36 (hg18) chr5: 17,661,439-176,508,326 SNX24, ADRA1B, 2152 more genes
    nsv3886795copy number variation1nstd102humanUncertain significance GRCh37 (hg19) chr5: 120,032,407-123,896,355 , GRCh38.p12 chr5: 120,696,712-124,560,662 , NCBI36 (hg18) chr5: 120,060,306-123,924,254 SNX24, PRR16, 41 more genes
    nsv3886374copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028 , NCBI36 (hg18) chr5: 66,648-180,837,635 SNX24, ADCY2, 2588 more genes
    nsv3884357copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr5: 86,400,000-154,000,000 , GRCh38.p12 chr5: 87,104,183-154,620,440 , NCBI36 (hg18) chr5: 86,435,756-153,980,193 SNX24, APC, 986 more genes
    nsv3884335copy number variation1nstd102humanUncertain significance GRCh37 (hg19) chr5: 122,050,926-122,346,676 , GRCh38.p12 chr5: 122,715,231-123,010,981 , NCBI36 (hg18) chr5: 122,078,825-122,374,575 SNX24, LOC105379154, 2 more genes
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