U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 14

    loading data ...

    Number of Variants: 14

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3871174copy number variation1nstd102humanBenign GRCh37 chr1: 38,031,972-38,105,212 , GRCh38.p12 chr1: 37,566,371-37,639,540 DNALI1, GNL2, 1 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 MARK1, LINC02766, 4930 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 SNAP47, STK40, 4927 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 RNU1-153P, MIR3917, 4887 more genes
    nsv3901163copy number variation1nstd102humanPathogenic GRCh37 chr1: 24,707,696-41,886,350 , GRCh38 chr1: 24,381,206-41,401,517 , NCBI36 chr1: 24,580,283-41,658,937 TMEM222, ZBTB8OS, 453 more genes
    nsv6313688copy number variation1nstd102humanPathogenic GRCh37 chr1: 33,285,582-47,891,811 , GRCh38.p12 chr1: 32,819,981-47,426,139 LOC107984940, PPIAP36, 407 more genes
    nsv3886123copy number variation1nstd102humanLikely benign GRCh37 chr1: 37,766,562-38,727,114 , GRCh38.p12 chr1: 37,300,961-38,261,442 FHL3, DNALI1, 36 more genes
    nsv3883497copy number variation1nstd102humanUncertain significance GRCh37 chr1: 38,001,813-38,068,791 , GRCh38.p12 chr1: 37,536,212-37,603,190 DNALI1, SNIP1, 4 more genes
    nsv3871383copy number variation1nstd102humanUncertain significance GRCh37 chr1: 38,001,813-38,043,237 , GRCh38.p12 chr1: 37,536,212-37,577,636 DNALI1, GNL2, 4 more genes
    nsv6313765copy number variation1nstd102humanUncertain significance GRCh37 chr1: 36,041,366-39,112,237 , GRCh38.p12 chr1: 35,575,765-38,646,565 RNU6-510P, AGO3, 78 more genes
    nsv3873946copy number variation1nstd102humanUncertain significance GRCh37 chr1: 38,005,705-38,077,489 , GRCh38.p12 chr1: 37,540,104-37,611,817 RPS27P9, FTH1P1, 5 more genes
    nsv4436181copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532 LINC01776, IGSF21-AS1, 1853 more genes
    nsv3878135copy number variation1nstd102humanUncertain significance GRCh37 chr1: 33,241,563-46,663,513 , GRCh38.p12 chr1: 32,775,962-46,197,841 LINC02786, LOC105378678, 365 more genes
    nsv7095992copy number variation1nstd102humanUncertain significance GRCh37 chr1: 38,003,349-38,273,852 , GRCh38.p12 chr1: 37,537,748-37,808,180 LOC105378650, ACTN4P2, 15 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Find related data

    Search details

    See more...

    Recent activity

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    Support Center