U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 24

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3919703copy number variation1nstd102humanUncertain significance NCBI36 chr7: 66,018,580-66,111,878 , GRCh37.p13 chr7: 66,381,145-66,474,443 , GRCh38.p12 chr7: 66,916,158-67,009,456 TMEM248, TYW1, 2 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 TMEM248, RNU6-438P, 2682 more genes
    nsv3888815copy number variation1nstd102humanPathogenic GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467 TMEM248, LOC107986817, 2014 more genes
    nsv3917508copy number variation1nstd102humanPathogenic GRCh37 chr7: 62,196,742-75,061,986 , GRCh38 chr7: 62,736,364-75,432,710 , NCBI36 chr7: 61,834,177-74,899,922 TMEM248, GTF2IP4, 285 more genes
    nsv3923428copy number variation1nstd102humanPathogenic GRCh38 chr7: 64,657,050-72,243,063 , NCBI36 chr7: 63,754,863-71,345,984 , GRCh37 chr7: 64,117,428-71,708,048 TMEM248, LOC402279, 112 more genes
    nsv3906315copy number variation1nstd102humanPathogenic GRCh37 chr7: 63,583,563-71,047,246 , GRCh38.p12 chr7: 64,123,185-71,582,261 TMEM248, LINC01372, 133 more genes
    nsv3894780copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842 TMEM248, RNU6-565P, 2684 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 TMEM248, RPL23AP51, 2684 more genes
    nsv3909087copy number variation1nstd102humanPathogenic GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620 TMEM248, MNX1-AS2, 2682 more genes
    nsv3908592copy number variation2nstd102humanPathogenic GRCh37 chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017 TMEM248, TRGV3, 2682 more genes
    nsv3915047copy number variation1nstd102humanPathogenic GRCh37 chr7: 53,341,752-68,041,200 , NCBI36 chr7: 53,309,246-67,679,136 , GRCh38 chr7: 53,274,059-68,576,213 TMEM248, VN1R25P, 333 more genes
    nsv3913119copy number variation1nstd102humanPathogenic NCBI36 chr7: 62,074,898-74,882,566 , GRCh38 chr7: 62,977,085-75,415,352 , GRCh37 chr7: 62,437,463-75,044,630 TMEM248, ARAFP1, 285 more genes
    nsv3915165copy number variation1nstd102humanPathogenic GRCh38 chr7: 62,570,287-67,823,956 , NCBI36 chr7: 61,668,100-66,926,378 , GRCh37 chr7: 62,030,665-67,288,943 TMEM248, VN1R34P, 169 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 TMEM248, AOC1, 2682 more genes
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 TMEM248, ACHE, 1532 more genes
    nsv6312786copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 65,556,983-66,460,414 , GRCh38.p12 chr7: 66,091,996-66,995,427 TMEM248, ASL, 27 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 TMEM248, RRBP1P1, 2680 more genes
    nsv3905746copy number variation1nstd102humanUncertain significance GRCh37 chr7: 66,082,383-67,559,054 , GRCh38.p12 chr7: 66,617,396-68,094,067 TMEM248, LOC107986741, 23 more genes
    nsv6291337copy number variation1nstd102humanUncertain significance GRCh37 chr7: 66,288,000-66,818,352 , GRCh38.p12 chr7: 66,823,013-67,353,365 TMEM248, RNU6-1254P, 13 more genes
    nsv3898103copy number variation1nstd102humanUncertain significance GRCh37 chr7: 65,470,729-66,599,216 , GRCh38.p12 chr7: 66,005,742-67,134,229 TMEM248, KCTD7, 31 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center