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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv2768222copy number variation1nstd125human GRCh37 chr5: 88,921,368-88,960,399 , GRCh38.p12 chr5: 89,625,551-89,664,582 LINC02161
    nsv2768224copy number variation1nstd125human GRCh37 chr6: 66,019,907-70,983,742 , GRCh38.p12 chr6: 65,310,014-70,274,039 ADGRB3, COL9A1, 29 more genes
    nsv2768227copy number variation1nstd125human GRCh37 chr9: 93,173,989-96,115,678 , GRCh38.p12 chr9: 90,411,707-93,353,396 AUH, ECM2, 68 more genes
    nsv2768201copy number variation3nstd125human GRCh37 chr2: 111,388,618-113,111,856 , GRCh38.p12 chr2: 110,631,041-112,354,279 BUB1, BCL2L11, 31 more genes
    nsv2768226copy number variation1nstd125human GRCh37 chr7: 45,373,134-47,029,521 , GRCh38.p12 chr7: 45,333,535-46,989,923 ADCY1, IGFBP1, 24 more genes
    nsv2768200copy number variation3nstd125human GRCh37 chr2: 109,147,410-110,492,659 , GRCh38.p12 chr2: 108,530,954-109,735,082 LIMS1, RANBP2, 21 more genes
    nsv2768225complex substitution1nstd125human GRCh37 chr7: 260,911-159,078,512 , GRCh38.p12 chr7: 242,519-159,285,823 AOC1, ACHE, 2762 more genes
    nsv2768202complex substitution2nstd125human GRCh37 chrX: 169,921-155,233,731 , GRCh38.p12 chrX: 253,254-156,004,066 ABCB7, ACTG1P10, 2192 more genes
    nsv2768204copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr16: 569,967-35,986,173 , GRCh37 chr16: 619,967-35,220,544 ABAT, ABCA3, 1043 more genes
    nsv2768219copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr19: 260,911-20,692,745 , GRCh37 chr19: 260,911-20,875,551 ACP5, TLE5, 914 more genes
    nsv2768218copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr19: 260,911-19,745,645 , GRCh37 chr19: 260,911-19,856,454 ACP5, TLE5, 867 more genes
    nsv2768217copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr19: 260,911-16,062,156 , GRCh37 chr19: 260,911-16,172,966 ACP5, TLE5, 724 more genes
    nsv2768229copy-neutral loss of heterozygosity1nstd125human GRCh37 chr3: 39,873,604-53,004,620 , GRCh38.p12 chr3: 39,832,113-52,970,604 ACY1, ALAS1, 400 more genes
    nsv2768220copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr19: 5,092,438-17,933,476 , GRCh37 chr19: 5,092,449-18,044,285 ACP5, GET3, 562 more genes
    nsv2768203copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr1: 47,200,473-54,167,957 , GRCh37 chr1: 47,666,145-54,633,630 CDKN2C, CPT2, 147 more genes
    nsv2768230copy-neutral loss of heterozygosity1nstd125human GRCh37 chr3: 46,715,645-52,852,488 , GRCh38.p12 chr3: 46,674,155-52,818,472 ACY1, ALAS1, 240 more genes
    nsv2768232copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr4: 158,719,122-164,075,078 , GRCh37 chr4: 159,640,274-164,996,230 NPY1R, NPY5R, 35 more genes
    nsv2768216copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr13: 73,851,090-79,043,551 , GRCh37 chr13: 74,425,227-79,617,686 BTF3P11, CLN5, 72 more genes
    nsv2768214copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr12: 84,704,059-89,082,002 , GRCh37 chr12: 85,097,838-89,475,779 GADD45AP1, KITLG, 38 more genes
    nsv2768205copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr16: 35,880-3,872,548 , GRCh37 chr16: 85,880-3,922,549 ABCA3, ARHGDIG, 274 more genes
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