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Items: 1 to 20 of 81

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7042468inversion1nstd229human GRCh38 chr5: 58,424,389-58,571,136 , GRCh37.p13 chr5: 57,720,216-57,866,963 MIR548AE2, GAPT, 2 more genes
    nsv6772768copy number variation1nstd229human GRCh38 chr5: 58,136,555-58,493,807 , GRCh37.p13 chr5: 57,432,382-57,789,634 LOC105378984, PLK2, 3 more genes
    nsv6770039copy number variation1nstd229human GRCh38 chr5: 58,457,001-58,583,600 , GRCh37.p13 chr5: 57,752,828-57,879,427 PLK2, RAB3C, 3 more genes
    nsv6769460copy number variation1nstd229human GRCh38 chr5: 58,434,576-58,473,455 , GRCh37.p13 chr5: 57,730,403-57,769,282 PLK2
    nsv6766352copy number variation1nstd229human GRCh38 chr5: 52,086,933-59,394,572 , GRCh37.p13 chr5: 51,382,767-58,690,398 , LOC105378980, 102 more genes
    nsv6765097copy number variation1nstd229human GRCh38 chr5: 57,933,632-58,641,442 , GRCh37.p13 chr5: 57,229,459-57,937,269 MIR548AE2, LOC105378984, 7 more genes
    nsv6403132copy number variation1nstd223human GRCh38 chr5: 58,434,576-58,473,460 , GRCh37.p13 chr5: 57,730,403-57,769,287 PLK2
    nsv6135669copy number variation1nstd213human GRCh37 chr5: 49,470,000-58,470,001 , GRCh38.p12 chr5: 50,174,166-59,174,175 , ASS1P9, 120 more genes
    nsv6135416copy number variation1nstd213human GRCh37 chr5: 50,510,000-68,870,001 , GRCh38.p12 chr5: 51,214,166-69,574,174 , TRIM23, 243 more genes
    nsv6135185copy number variation1nstd213human GRCh37 chr5: 57,140,000-58,050,001 , GRCh38.p12 chr5: 57,844,173-58,754,174 GAPT, LINC02101, 8 more genes
    nsv5465476copy number variation1nstd206human GRCh38 chr5: 57,931,909-58,692,386 , GRCh37.p13 chr5: 57,227,736-57,988,213 PLK2, RAB3C, 7 more genes
    nsv5313375copy number variation1nstd204human GRCh37.p13 chr5: 57,227,752-57,988,202 , GRCh38.p13 chr5: 57,931,925-58,692,375 PLK2, RAB3C, 7 more genes
    nsv5221686copy number variation1nstd204human GRCh38.p13 chr5: 58,390,301-58,563,100 , GRCh37.p13 chr5: 57,686,128-57,858,927 LINC02108, LOC105378984, 3 more genes
    nsv4948789copy number variation1nstd200human GRCh38 chr5: 57,931,929-58,692,366 , GRCh37.p13 chr5: 57,227,756-57,988,193 LOC105378984, PLK2, 7 more genes
    nsv4523070copy number variation1nstd166human GRCh37.p13 chr5: 57,245,997-58,257,000 , GRCh38.p12 chr5: 57,950,170-58,961,173 GAPT, MIR548AE2, 8 more genes
    nsv4456295copy number variation1nstd102humanUncertain significance GRCh37 chr5: 56,283,070-58,079,028 , GRCh38.p12 chr5: 56,987,243-58,783,201 SALL4P1, LINC02225, 17 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4119813copy number variation1nstd166human GRCh37.p13 chr5: 39,131,458-67,637,618 , GRCh38.p12 chr5: 39,131,356-68,341,790 , ESM1, 305 more genes
    nsv3923429copy number variation1nstd102humanPathogenic GRCh37 chr5: 49,584,189-62,445,597 , NCBI36 chr5: 49,619,946-62,481,353 , GRCh38 chr5: 50,288,355-63,149,770 ISCA1P1, LOC643307, 163 more genes
    nsv3920391copy number variation1nstd102humanPathogenic GRCh38 chr5: 35,201,559-61,903,141 , GRCh37 chr5: 35,201,661-61,198,968 , NCBI36 chr5: 35,237,418-61,234,725 KRT18P56, LINC01265, 290 more genes
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