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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7079658copy number variation1nstd229human GRCh38 chrX: 152,736,201-152,740,700 , GRCh37.p13 chrX|NW_003871103.3: 170,184-174,683 , GRCh37.p13 chrX: 151,896,261-151,900,761 MAGEA12, CSAG4
    esv3664853complex substitution1estd217human GRCh37 chrX: 151,898,729-151,898,836 , GRCh38.p12 chrX: 152,738,126-152,738,233 MAGEA12, CSAG4
    nsv3193261copy number variation2nstd152human GRCh37.p13 chrX|NW_003871103.3: 152,762-183,668 , GRCh38 chrX: 152,718,779-152,749,685 , GRCh37.p13 chrX: 151,887,274-151,918,215 MAGEA12, MAGEA2, 3 more genes
    nsv4047165copy number variation1nstd166human GRCh37.p13 chrX: 151,894,041-151,905,316 , GRCh38.p12 chrX: 152,731,648-152,738,707 MAGEA12, CSAG1, 1 more genes
    nsv2767219copy number variation1nstd130human NCBI36 chrX: 151,645,989-151,660,146 , GRCh37.p13 chrX|NW_003871103.3: 161,495-175,611 , GRCh37.p13 chrX: 151,895,333-151,909,490 , GRCh38.p12 chrX: 152,729,754-152,738,707 MAGEA12, CSAG1, 1 more genes
    nsv3415821insertion2nstd162human GRCh37.p13 chrX|NW_003871103.3: 166,351-166,351 , GRCh38 chrX: 152,732,368-152,732,368 , GRCh37.p13 chrX: 151,904,595-151,904,595 MAGEA12, CSAG1, 1 more genes
    nsv3412949insertion1nstd162human GRCh37.p13 chrX|NW_003871103.3: 166,341-166,341 , GRCh38 chrX: 152,732,358-152,732,358 , GRCh37.p13 chrX: 151,904,605-151,904,605 MAGEA12, CSAG1, 1 more genes
    nsv6147165inversion1nstd206human GRCh37.p13 chrX|NW_003871103.3: 159,042-177,359 , GRCh38 chrX: 152,725,059-152,743,376 , GRCh37.p13 chrX: 151,893,731-151,912,089 MAGEA12, CSAG1, 1 more genes
    nsv5665135inversion1nstd207human GRCh37.p13 chrX: 151,898,256-151,907,247 , GRCh38 chrX: 152,729,755-152,738,706 , GRCh37.p13 chrX|NW_003871103.3: 163,738-172,689 MAGEA12, CSAG1, 1 more genes
    nsv5969201inversion1nstd209human GRCh37.p13 chrX: 151,894,141-151,911,353 , GRCh38 chrX: 152,725,649-152,742,820 , GRCh37.p13 chrX|NW_003871103.3: 159,632-176,803 MAGEA12, CSAG1, 1 more genes
    nsv3188296complex substitution2nstd152human GRCh37.p13 chrX|NW_003871103.3: 141,426-177,986 , GRCh38 chrX: 152,707,443-152,744,003 , GRCh37.p13 chrX: 151,892,958-151,929,556 MAGEA12, CSAG1, 3 more genes
    nsv3904162copy number variation1nstd102humanPathogenic GRCh38 chrX: 10,001-156,030,895 , GRCh37 chrX: 60,001-155,260,560 , NCBI36 chrX: 1-154,913,754 MAGEA12, NANOGNBP3, 2154 more genes
    nsv3913255copy number variation2nstd102humanPathogenic NCBI36 chrX: 701-154,913,754 , GRCh37.p13 chrX: 60,701-155,260,560 , GRCh38.p12 chrX: 10,701-156,030,895 MAGEA12, NHS-AS1, 2154 more genes
    nsv3907094copy number variation4nstd102humanPathogenic GRCh38 chrX: 10,679-156,022,206 , GRCh37 chrX: 60,679-155,251,871 , NCBI36 chrX: 679-154,905,065 MAGEA12, GPR119, 2153 more genes
    nsv3878553copy number variation2nstd102humanPathogenic GRCh37 chrX: 60,262-155,245,765 , GRCh38.p12 chrX: 10,262-156,016,100 MAGEA12, H2AB2, 2152 more genes
    nsv3898149copy number variation1nstd102humanPathogenic GRCh38 chrX: 20,297-156,026,127 , NCBI36 chrX: 10,297-154,908,986 , GRCh37 chrX: 70,297-155,255,792 MAGEA12, OR3B1P, 2154 more genes
    nsv3877395copy number variation1nstd102humanPathogenic GRCh37 chrX: 71,267-155,255,839 , GRCh38.p12 chrX: 21,267-156,026,174 MAGEA12, ARMCX2, 2154 more genes
    nsv3884935copy number variation1nstd102humanPathogenic GRCh37 chrX: 71,267-155,255,792 , GRCh38.p12 chrX: 21,267-156,026,127 MAGEA12, NDUFB11, 2154 more genes
    nsv3903061copy number variation1nstd102humanPathogenic NCBI36 chrX: 679-154,896,026 , GRCh38 chrX: 10,679-156,013,167 , GRCh37 chrX: 60,679-155,242,832 MAGEA12, SLC38A5, 2152 more genes
    nsv3885865copy number variation1nstd102humanPathogenic GRCh37 chrX: 70,297-155,246,585 , GRCh38.p12 chrX: 20,297-156,016,920 MAGEA12, MIR1277, 2152 more genes
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