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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7042607inversion1nstd229human GRCh38 chr6: 77,435,338-77,462,780 , GRCh37.p13 chr6: 78,145,055-78,172,497 LOC105377864, HTR1B
    nsv6781783copy number variation1nstd229human GRCh38 chr6: 77,450,189-77,462,762 , GRCh37.p13 chr6: 78,159,906-78,172,479 HTR1B, LOC105377864
    nsv6636747copy number variation1nstd102humanUncertain significance GRCh37 chr6: 77,773,778-80,880,138 , GRCh38.p12 chr6: 77,064,061-80,170,421 TRF-GAA8-1, HMGN3-AS1, 31 more genes
    nsv6315402copy number variation1nstd102humanPathogenic GRCh37 chr6: 64,954,687-79,581,678 , GRCh38.p12 chr6: 64,244,794-78,871,961 LOC105377841, RPS6P8, 139 more genes
    nsv6313857copy number variation1nstd102humanPathogenic GRCh37 chr6: 69,938,252-94,379,210 , GRCh38.p12 chr6: 69,228,360-93,669,492 LOC101928570, RNU4-72P, 288 more genes
    nsv6313791copy number variation1nstd102humanUncertain significance GRCh37 chr6: 76,680,462-78,260,898 , GRCh38.p12 chr6: 75,970,745-77,551,181 IMPG1, LOC101928570, 10 more genes
    nsv6291339copy number variation1nstd102humanPathogenic GRCh37 chr6: 70,165,296-79,920,769 , GRCh38.p12 chr6: 69,455,404-79,211,052 RNU6-84P, PGAM1P10, 113 more genes
    nsv6291322copy number variation1nstd102humanPathogenic GRCh37 chr6: 72,799,054-83,275,894 , GRCh38.p12 chr6: 72,089,351-82,566,177 RPS27P15, COX7A2, 118 more genes
    nsv4729340copy number variation1nstd102humanPathogenic GRCh37 chr6: 74,226,559-80,208,037 , GRCh38.p12 chr6: 73,516,836-79,498,320 LOC107986613, LOC101928516, 58 more genes
    nsv4611893copy number variation1nstd183human GRCh37 chr6: 77,589,231-78,258,249 , GRCh38.p12 chr6: 76,879,514-77,548,532 RPS6P7, LOC105377864, 3 more genes
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 HLA-DPB2, CIMIP3, 1001 more genes
    nsv3924180copy number variation1nstd102humanPathogenic NCBI36 chr6: 65,316,269-84,193,229 , GRCh38 chr6: 64,549,655-83,426,791 , GRCh37 chr6: 65,259,548-84,136,510 LOC105377875, KCNQ5-IT1, 188 more genes
    nsv3921478copy number variation1nstd102humanPathogenic NCBI36 chr6: 76,692,636-93,477,232 , GRCh38 chr6: 75,926,199-92,710,793 , GRCh37 chr6: 76,635,916-93,420,511 SPACA1, TAF13P1, 187 more genes
    nsv3919111copy number variation1nstd102humanPathogenic GRCh38 chr6: 74,382,807-142,040,500 , NCBI36 chr6: 75,149,243-142,403,330 , GRCh37 chr6: 75,092,523-142,361,637 RNU6-770P, MAP3K5-AS2, 810 more genes
    nsv3916197copy number variation1nstd102humanUncertain significance NCBI36 chr6: 77,821,294-78,408,713 , GRCh38 chr6: 77,054,858-77,642,277 , GRCh37 chr6: 77,764,575-78,351,994 HTR1B, LOC105377862, 3 more genes
    nsv3889959copy number variation1nstd102humanPathogenic GRCh37 chr6: 73,674,612-84,829,774 , GRCh38.p12 chr6: 72,964,889-84,120,055 MRAP2, LCA5, 125 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 ITPR3, HSD17B8, 2905 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 SOD1P1, HLA-DPB1, 2905 more genes
    nsv3884234copy number variation1nstd102humanUncertain significance GRCh37 chr6: 77,755,256-78,440,782 , GRCh38.p12 chr6: 77,045,539-77,731,065 LOC101928570, RPS6P7, 4 more genes
    nsv3884009copy number variation1nstd102humanUncertain significance GRCh37 chr6: 77,841,102-79,060,009 , GRCh38.p12 chr6: 77,131,385-78,350,292 LOC101928570, LOC105377865, 4 more genes
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