ClinVar Miner

List of variants in gene INVS reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (913):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 65
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HGVS dbSNP
NC_000009.11:g.(?_102988324)_(102988537_?)del
NM_001318381.1(INVS):c.2494C>T (p.Arg832Ter) rs376879175
NM_014425.5(INVS):c.*466_*467CA[18] rs10527613
NM_014425.5(INVS):c.*466_*467CA[19] rs10527613
NM_014425.5(INVS):c.*466_*467CA[21] rs10527613
NM_014425.5(INVS):c.*466_*467CA[23] rs10527613
NM_014425.5(INVS):c.*466_*467insTCAC rs200314659
NM_014425.5(INVS):c.*466_*467insTCACAC rs200314659
NM_014425.5(INVS):c.*469A>T rs886063279
NM_014425.5(INVS):c.*73T>A rs886063273
NM_014425.5(INVS):c.*98A>G rs886063274
NM_014425.5(INVS):c.-129C>A rs533889420
NM_014425.5(INVS):c.-155C>T rs62577237
NM_014425.5(INVS):c.-178G>A rs886063263
NM_014425.5(INVS):c.1111A>G (p.Ser371Gly) rs200546215
NM_014425.5(INVS):c.118C>G (p.Leu40Val) rs148219510
NM_014425.5(INVS):c.1220A>C (p.Gln407Pro)
NM_014425.5(INVS):c.1317C>T (p.Cys439=) rs886063266
NM_014425.5(INVS):c.1379T>G (p.Leu460Trp) rs878854980
NM_014425.5(INVS):c.1396G>A (p.Gly466Arg) rs1554726564
NM_014425.5(INVS):c.1464+1G>A rs375753623
NM_014425.5(INVS):c.1466G>A (p.Gly489Glu) rs1015507237
NM_014425.5(INVS):c.1490G>A (p.Cys497Tyr) rs1296545586
NM_014425.5(INVS):c.1571+2dup rs1554728033
NM_014425.5(INVS):c.1899_1901CAG[1] (p.Ser634del) rs886063267
NM_014425.5(INVS):c.1913G>A (p.Arg638Gln) rs761806481
NM_014425.5(INVS):c.1916C>A (p.Ala639Asp) rs886063268
NM_014425.5(INVS):c.1943A>G (p.Asn648Ser) rs116686341
NM_014425.5(INVS):c.1945G>A (p.Val649Met) rs115042730
NM_014425.5(INVS):c.2001C>T (p.Gly667=) rs536554704
NM_014425.5(INVS):c.2009T>C (p.Leu670Pro) rs762112247
NM_014425.5(INVS):c.2056A>G (p.Arg686Gly) rs150001738
NM_014425.5(INVS):c.2116A>G (p.Arg706Gly) rs116222916
NM_014425.5(INVS):c.2152G>C (p.Gly718Arg) rs1554730698
NM_014425.5(INVS):c.2200C>T (p.Arg734Trp) rs370949695
NM_014425.5(INVS):c.2232G>C (p.Gln744His)
NM_014425.5(INVS):c.2260G>A (p.Asp754Asn) rs115401137
NM_014425.5(INVS):c.2279C>T (p.Ser760Phe)
NM_014425.5(INVS):c.2285G>A (p.Arg762Gln)
NM_014425.5(INVS):c.2310C>T (p.His770=) rs116606949
NM_014425.5(INVS):c.2335C>T (p.Arg779Trp) rs370643191
NM_014425.5(INVS):c.2380C>T (p.Arg794Cys) rs556807161
NM_014425.5(INVS):c.2386C>G (p.Gln796Glu) rs147731667
NM_014425.5(INVS):c.2428C>T (p.Arg810Cys) rs984016152
NM_014425.5(INVS):c.2441C>T (p.Ala814Val) rs886063269
NM_014425.5(INVS):c.2443C>T (p.Arg815Trp) rs564509196
NM_014425.5(INVS):c.2453C>T (p.Ala818Val)
NM_014425.5(INVS):c.2489C>T (p.Thr830Ile) rs886063270
NM_014425.5(INVS):c.2776G>A (p.Ala926Thr) rs374891838
NM_014425.5(INVS):c.2819G>A (p.Arg940Gln)
NM_014425.5(INVS):c.284G>A (p.Arg95His) rs372088206
NM_014425.5(INVS):c.2874A>G (p.Thr958=) rs886063271
NM_014425.5(INVS):c.3027C>T (p.His1009=) rs201136636
NM_014425.5(INVS):c.3056C>G (p.Ser1019Cys) rs886063272
NM_014425.5(INVS):c.3099C>T (p.Asn1033=) rs368303175
NM_014425.5(INVS):c.3182dup (p.Asn1061fs) rs760013326
NM_014425.5(INVS):c.564G>A (p.Trp188Ter) rs1564167474
NM_014425.5(INVS):c.740A>G (p.Asn247Ser) rs41312220
NM_014425.5(INVS):c.775C>T (p.Leu259=) rs886063264
NM_014425.5(INVS):c.796+4C>T rs371310920
NM_014425.5(INVS):c.889G>A (p.Ala297Thr) rs116475199
NM_014425.5(INVS):c.907-13dup rs750082874
NM_014425.5(INVS):c.907-7C>G
NM_014425.5(INVS):c.916A>G (p.Lys306Glu) rs878854981
NM_014425.5(INVS):c.962A>G (p.Glu321Gly)

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